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  • Sleep State Misperception Wikipedia
    Sleep state misperception Other names Paradoxical insomnia, pseudo-insomnia, subjective insomnia, subjective sleepiness, sleep hypochondriasis [1] Specialty Sleep medicine Sleep state misperception ( SSM ) is a term in the International Classification of Sleep Disorders (ICSD) most commonly used for people who mistakenly perceive their sleep as wakefulness, [1] [2] though it has been proposed that it be applied to those who severely overestimate their sleep time as well [3] ("positive" sleep state misperception). [4] While most sleepers with this condition will report not having slept in the previous night at all or having slept very little, [5] clinical recordings generally show normal sleep patterns. ... Philadelphia: WB Saunders, 1994. [ page needed ] External links [ edit ] Classification D ICD - 10 : F51.0 , G47.0 ICD - 9-CM : 307.42 , 307.49 , 780.52 MeSH : D020919 DiseasesDB : 26877 SNOMED CT : 427745001 External resources eMedicine : med/2698 v t e Sleep and sleep disorders Stages of sleep cycles Rapid eye movement (REM) Non-rapid eye movement Slow-wave Brain waves Alpha wave Beta wave Delta wave Gamma wave K-complex Mu rhythm PGO waves Sensorimotor rhythm Sleep spindle Theta wave Sleep disorders Dyssomnia Excessive daytime sleepiness Hypersomnia Insomnia Kleine–Levin syndrome Narcolepsy Night eating syndrome Nocturia Sleep apnea Catathrenia Central hypoventilation syndrome Obesity hypoventilation syndrome Obstructive sleep apnea Periodic breathing Sleep state misperception Circadian rhythm disorders Advanced sleep phase disorder Cyclic alternating pattern Delayed sleep phase disorder Irregular sleep–wake rhythm Jet lag Non-24-hour sleep–wake disorder Shift work sleep disorder Parasomnia Bruxism Nightmare disorder Night terror Periodic limb movement disorder Rapid eye movement sleep behavior disorder Sleepwalking Somniloquy Benign phenomena Dreams Exploding head syndrome Hypnic jerk Hypnagogia / Sleep onset Hypnopompic state Sleep paralysis Sleep inertia Somnolence Nocturnal clitoral tumescence Nocturnal penile tumescence Nocturnal emission Treatment Sleep diary Sleep hygiene Sleep induction Hypnosis Lullaby Somnology Polysomnography Other Sleep medicine Behavioral sleep medicine Sleep study Daily life Bed Bunk bed Daybed Four-poster bed Futon Hammock Mattress Sleeping bag Bed bug Bedding Bedroom Bedtime Bedtime story Bedtime toy Biphasic and polyphasic sleep Chronotype Dream diary Microsleep Mouth breathing Nap Nightwear Power nap Second wind Siesta Sleep and creativity Sleep and learning Sleep deprivation / Sleep debt Sleeping while on duty Sleepover Snoring
  • Rhythmic Movement Disorder Wikipedia
    This may be due to RMD’s comorbidity with sleep apnea, which has been observed in some patients [6] . ... Other sleep related disorders like sleep apnea are ruled out by examining the patients’ respiratory effort, air flow, and oxygen saturation. ... In some patients who also experience sleep apnea, episodes of apnea can be followed immediately by RMD-like symptoms, suggesting that the apnea episodes may trigger an RMD episode. ... Infantile and adolescent RMD respond well to low doses of clonazepam . [19] Prescription medications such as ropinirole or pramipexole given to restless legs syndrome patients do not show any clinical improvement in many patients with RMD. [6] Non-medication [ edit ] Treatment of sleep apnea via a continuous positive airway pressure ( CPAP ) device has shown dramatic improvement in apnea and nearly complete resolution of RMD symptoms. [7] Behavioral interventions may alleviate some RMD symptoms and movements. ... "Rhythmic movement disorder associated with respiratory arousals and improved by CPAP titration in a patient with restless legs syndrome and sleep apnea". Sleep Med . 10 (4): 501–3. doi : 10.1016/j.sleep.2009.03.003 .
  • Carotid Artery Disease Mayo_clinic
    Excess weight increases the chances of high blood pressure, atherosclerosis and diabetes. Sleep apnea. Spells of stopping breathing at night might increase the risk of stroke. ... Being overweight increases other risk factors, such as high blood pressure, cardiovascular disease, diabetes and sleep apnea. Eat a healthy diet. Focus on fruits and vegetables, whole grains and fish, nuts and legumes. ... What do you eat in a typical day? Do you have symptoms of sleep apnea?
    APOE, CCL2, HMOX1, GSTP1, TP53, PODXL, AGT, FASLG, MRAS, CD163, PLAU, AGER, LTB4R, PON1, IL6, LPA, PLTP, PLG, TNFSF4, NOS3, MTHFR, SLC39A2, SHOC1, MMP9, HGF, CRP, IL1RN, CCL18, SELE, SREBF2, TNF, ACE, CYP27A1, TNFRSF4, VLDLR, PTGES, REN, TOMM40, CD14, MMRN1, APOB, EGFL7, BTNL2, PSRC1, ALOX5, NANOS3, EDN1, PTGS2, IGF1, HSPD1, IL10, IL10RA, INS, LIPC, ICAM1, LRP1, MET, MMP3, MPO, PPARG, NFKB1, NFKBIA, GSTT1, GNB3, FGB, F5, F3, CELSR2, MIR126
  • Exploding Head Syndrome Wikipedia
    External links [ edit ] Classification D ICD - 10 : G47.59 v t e Sleep and sleep disorders Stages of sleep cycles Rapid eye movement (REM) Non-rapid eye movement Slow-wave Brain waves Alpha wave Beta wave Delta wave Gamma wave K-complex Mu rhythm PGO waves Sensorimotor rhythm Sleep spindle Theta wave Sleep disorders Dyssomnia Excessive daytime sleepiness Hypersomnia Insomnia Kleine–Levin syndrome Narcolepsy Night eating syndrome Nocturia Sleep apnea Catathrenia Central hypoventilation syndrome Obesity hypoventilation syndrome Obstructive sleep apnea Periodic breathing Sleep state misperception Circadian rhythm disorders Advanced sleep phase disorder Cyclic alternating pattern Delayed sleep phase disorder Irregular sleep–wake rhythm Jet lag Non-24-hour sleep–wake disorder Shift work sleep disorder Parasomnia Bruxism Nightmare disorder Night terror Periodic limb movement disorder Rapid eye movement sleep behavior disorder Sleepwalking Somniloquy Benign phenomena Dreams Exploding head syndrome Hypnic jerk Hypnagogia / Sleep onset Hypnopompic state Sleep paralysis Sleep inertia Somnolence Nocturnal clitoral tumescence Nocturnal penile tumescence Nocturnal emission Treatment Sleep diary Sleep hygiene Sleep induction Hypnosis Lullaby Somnology Polysomnography Other Sleep medicine Behavioral sleep medicine Sleep study Daily life Bed Bunk bed Daybed Four-poster bed Futon Hammock Mattress Sleeping bag Bed bug Bedding Bedroom Bedtime Bedtime story Bedtime toy Biphasic and polyphasic sleep Chronotype Dream diary Microsleep Mouth breathing Nap Nightwear Power nap Second wind Siesta Sleep and creativity Sleep and learning Sleep deprivation / Sleep debt Sleeping while on duty Sleepover Snoring
  • Pure Autonomic Failure Wikipedia
    More pervasive autonomic dysfunction involving any of the following: night sweats or abnormal lack of sweating, urogenital problems (frequent UTIs, incontinence, frequency, urgency), gastrointestinal problems (chronic constipation, chronic constipation alternating with diarrhea, poor gastric motility), or esophageal/respiratory problems ( sleep apnea , abnormal breath sounds during sleep or while awake) indicate possible autoimmune autonomic ganglionopathy or multiple system atrophy .
    SNCA, DBH, PRNP, SOD1, TPO, APP, GDNF, IGFALS, ATXN3, PLAU, THM, TTR
    • Multiple System Atrophy Medlineplus
      Multiple system atrophy is a progressive brain disorder that affects movement and balance and disrupts the function of the autonomic nervous system. The autonomic nervous system controls body functions that are mostly involuntary, such as regulation of blood pressure. The most frequent autonomic symptoms associated with multiple system atrophy are a sudden drop in blood pressure upon standing (orthostatic hypotension), urinary difficulties, and erectile dysfunction in men. Researchers have described two major types of multiple system atrophy, which are distinguished by their major signs and symptoms at the time of diagnosis. In one type, known as MSA-P, a group of movement abnormalities called parkinsonism are predominant.
    • Pure Autonomic Failure Gard
      Pure autonomic failure (PAF) is a neurodegenerative disease of the autonomic nervous system , which regulates body processes like blood pressure and breathing rate. PAF usually affects only the peripheral autonomic nervous system, which means it does not usually involve the brain and spinal cord (the central nervous system). Symptoms begin in midlife, although they can begin earlier. The main symptom of PAF is orthostatic hypotension , a sudden drop in blood pressure upon standing. This can cause dizziness, lightheadedness, blurry vision, and weakness. Other symptoms can include fatigue, bladder problems, constipation, abnormal sweating, and sleep disorders.
    • Pure Autonomic Failure Orphanet
      Ambulatory blood pressure monitoring can reveal a disappearance or reversal of the day/night rhythm. Specific tests for PAF (Ewing test, pupillary or sudoral function, analysis of heart rate and blood pressure variability, sympathetic microneurography and MIBG scintigraphy) are carried out by some laboratories. ... Decubitus arterial hypertension can be prevented by following simple rules (avoiding taking a vasoconstrictor before sleeping, resting in a semi-sitting position over night, taking an antihypertensive drug in extreme cases).
  • Mucopolysaccharidosis Type Ii Gene_reviews
    Additional studies may include: sleep study for obstructive apnea; nerve conduction velocity to assess for carpal tunnel syndrome; head/neck MRI to document ventricular size and cervicomedullary narrowing; opening pressure on lumbar puncture; and orthopedic evaluation to monitor hip disease. ... Retinal degeneration leads to poor peripheral vision and night blindness, which occur frequently in individuals with MPS II, while central visual impairment due to retinal degeneration is rare [Suppiej et al 2013]. ... Ear, Nose, Throat Common oral findings in boys with MPS II include macroglossia, hypertrophic adenoids and tonsils, and ankylosis of the temporomandibular joint, which limits opening of the mouth. ... The progression of airway obstruction is relentless and usually results in sleep apnea and the need for positive pressure assistance and eventually tracheostomy. ... Visualization of the vocal cords is compromised by the large tongue, GAG-infiltrated soft tissues, and large tonsils and adenoids. Care must be taken to avoid hyperextension of the neck secondary to atlantoaxial instability and cervicomedullary compression that may be present.
    IDS, ARSH, IDS2, TFRC, IDUA, LINC00893, MPEG1, TTK, RPS27, F9, FMR1, IDSP1, ABCB6, CD38, FOXG1, SLC35G1, ARNTL2, DESI1, CLOCK, L1CAM, PER2, AFF2, CD34, PER1, CD99, CANX
    • Mucopolysaccharidosis Type 2, Severe Form Orphanet
      Mucopolysaccharidosis type 2 (MPS2, see this term), severe form (MPS2S), is associated with a massive accumulation of glycosaminoglycans and a wide variety of symptoms including a rapidly progressive cognitive decline; it is most often fatal in the second or third decade. Epidemiology Prevalence of MPS2 at birth in Europe is 1/166,000, the severe form accounts for at least two-thirds of all cases. Clinical description MPS2S presents with the spectrum of symptoms observed in all MSP2 (see this term) cases, often with an earlier presentation. MPS2S patients have a decrease in growth rate in early to mid-childhood, along with respiratory difficulties and a thickening of lips and nostrils as well as an enlarged and protruding tongue (distinctive facies), which may become evident between 2-4 years of age. Psychomotor milestones are delayed, and regression often occurs. Between the ages of 2-6 years patients begin to exhibit aggressive behavior and hyperactivity, often lacking any sense of danger as they follow a course of progressive cognitive decline.
    • Mucopolysaccharidosis, Type Ii Omim
      Clinical Variability Patients with complete deletion of the IDS locus often have atypical phenotypes, including ptosis, obstructive sleep apnea, and seizures (Wraith et al., 1991; Froissart et al., 1993). ... INHERITANCE - X-linked recessive GROWTH Height - Dwarfism, mild - Adult height 120-150cm HEAD & NECK Head - Scaphocephaly - Macrocephaly Face - Coarse facies Ears - Hearing loss - Recurrent otitis media Eyes - No corneal opacities - Papilledema - Retinal pigmentation - Ptosis Nose - Mucoid nasal discharge Mouth - Macroglossia - Full lips Teeth - Delayed tooth eruption - Widely spaced teeth Neck - Short neck CARDIOVASCULAR Heart - Valvular heart disease - Ischemic heart disease - Congestive heart failure RESPIRATORY Airways - Tracheobronchomalacia - Obstructive sleep apnea - Asthma ABDOMEN External Features - Inguinal hernia - Umbilical hernia Liver - Hepatomegaly Spleen - Splenomegaly Gastrointestinal - Diarrhea - Intestinal pseudo-obstruction SKELETAL - Dysostosis multiplex Spine - Kyphosis Limbs - Flexion contractures Hands - Claw hand Feet - Pes cavus SKIN, NAILS, & HAIR Skin - Pebbly skin lesions on back, upper arms, and thigh Hair - Hypertrichosis NEUROLOGIC Central Nervous System - Neurodegeneration leading to profound mental retardation - Cervical cord compression - Hydrocephalus - Normal intelligence in IIB - Seizures VOICE - Hoarse voice LABORATORY ABNORMALITIES - Iduronate sulfatase deficiency in fibroblasts, amniocytes and white blood cells - Dermatan and heparan sulfate excretion in urine MISCELLANEOUS - Onset 2-4 years of age in IIA - Two forms: IIA (severe) and IIB (mild) - Death before age 15 in IIA - Survival to 20s-60s in IIB - Prenatal diagnosis available MOLECULAR BASIS - Caused by mutation in the iduronate-2-sulfatase gene (IDS, 309900.0001 ) ▲ Close
    • Mucopolysaccharidosis Type 2, Attenuated Form Orphanet
      Swelling of the upper respiratory tract may be responsible for frequent infections, in particular otitis media; excessive snoring and sleep apnea; a distinctive hoarse voice and progressive loss of hearing.
    • Mucopolysaccharidosis Type 2 Orphanet
      A lysosomal storage disease with multisystemic involvement leading to a massive accumulation of glycosaminoglycans and a wide variety of symptoms including distinctive coarse facial features, short stature, cardio-respiratory involvement and skeletal abnormalities. It manifests as a continuum varying from a severe form with neurodegeneration to an attenuated form without neuronal involvement. Epidemiology Mucopolysaccharidosis type 2 (MPS2) prevalence at birth in Europe is 1/166,000. It is an X-linked recessive disorder; very rare cases of female presentation have been reported. Clinical description MPS2 patients appear healthy at birth, with initial symptoms appearing between 18 months and 4 years of age.
    • Mucopolysaccharidosis Type Ii Medlineplus
      Narrowing of the airway causes frequent upper respiratory infections and short pauses in breathing during sleep (sleep apnea). As the disorder progresses, individuals need medical assistance to keep their airway open.
    • Mucopolysaccharidosis Type Ii Gard
      Mucopolysaccharidosis II (MPS II) is an inherited disorder of carbohydrate metabolism that occurs almost exclusively in males. It is characterized by distinctive facial features, a large head, hydrocephalus, enlargement of the liver and spleen (hepatosplenomegaly), umbilical or inguinal hernia , and hearing loss. Individuals with this condition may additionally have joint deformities and heart abnormalities involving the valves. MPS II is caused by mutations in the IDS gene and is inherited in an X-linked manner. There is a wide range in severity of symptoms present in individuals with MPS II.
  • Laryngospasm Wikipedia
    ., "Laryngospam -The Best Treatment", Anesthesiology , 11 1998, Vol.89, 1293–1294 v t e Diseases of the respiratory system Upper RT (including URTIs , common cold ) Head sinuses Sinusitis nose Rhinitis Vasomotor rhinitis Atrophic rhinitis Hay fever Nasal polyp Rhinorrhea nasal septum Nasal septum deviation Nasal septum perforation Nasal septal hematoma tonsil Tonsillitis Adenoid hypertrophy Peritonsillar abscess Neck pharynx Pharyngitis Strep throat Laryngopharyngeal reflux (LPR) Retropharyngeal abscess larynx Croup Laryngomalacia Laryngeal cyst Laryngitis Laryngopharyngeal reflux (LPR) Laryngospasm vocal cords Laryngopharyngeal reflux (LPR) Vocal fold nodule Vocal fold paresis Vocal cord dysfunction epiglottis Epiglottitis trachea Tracheitis Laryngotracheal stenosis Lower RT / lung disease (including LRTIs ) Bronchial / obstructive acute Acute bronchitis chronic COPD Chronic bronchitis Acute exacerbation of COPD ) Asthma ( Status asthmaticus Aspirin-induced Exercise-induced Bronchiectasis Cystic fibrosis unspecified Bronchitis Bronchiolitis Bronchiolitis obliterans Diffuse panbronchiolitis Interstitial / restrictive ( fibrosis ) External agents/ occupational lung disease Pneumoconiosis Aluminosis Asbestosis Baritosis Bauxite fibrosis Berylliosis Caplan's syndrome Chalicosis Coalworker's pneumoconiosis Siderosis Silicosis Talcosis Byssinosis Hypersensitivity pneumonitis Bagassosis Bird fancier's lung Farmer's lung Lycoperdonosis Other ARDS Combined pulmonary fibrosis and emphysema Pulmonary edema Löffler's syndrome / Eosinophilic pneumonia Respiratory hypersensitivity Allergic bronchopulmonary aspergillosis Hamman-Rich syndrome Idiopathic pulmonary fibrosis Sarcoidosis Vaping-associated pulmonary injury Obstructive / Restrictive Pneumonia / pneumonitis By pathogen Viral Bacterial Pneumococcal Klebsiella Atypical bacterial Mycoplasma Legionnaires' disease Chlamydiae Fungal Pneumocystis Parasitic noninfectious Chemical / Mendelson's syndrome Aspiration / Lipid By vector/route Community-acquired Healthcare-associated Hospital-acquired By distribution Broncho- Lobar IIP UIP DIP BOOP-COP NSIP RB Other Atelectasis circulatory Pulmonary hypertension Pulmonary embolism Lung abscess Pleural cavity / mediastinum Pleural disease Pleuritis/pleurisy Pneumothorax / Hemopneumothorax Pleural effusion Hemothorax Hydrothorax Chylothorax Empyema/pyothorax Malignant Fibrothorax Mediastinal disease Mediastinitis Mediastinal emphysema Other/general Respiratory failure Influenza Common cold SARS Coronavirus disease 2019 Idiopathic pulmonary haemosiderosis Pulmonary alveolar proteinosis v t e Underwater diving Diving modes Atmospheric pressure diving Freediving Saturation diving Scuba diving Snorkeling Surface oriented diving Surface-supplied diving Unmanned diving Diving equipment Cleaning and disinfection of personal diving equipment Human factors in diving equipment design Basic equipment Diving mask Snorkel Swimfin Breathing gas Bailout gas Bottom gas Breathing air Decompression gas Emergency gas supply Heliox Nitrox Oxygen Travel gas Trimix Buoyancy and trim equipment Buoyancy compensator Power inflator Dump valve Diving weighting system Ankle weights Integrated weights Trim weights Weight belt Decompression equipment Decompression buoy Decompression cylinder Decompression trapeze Dive computer Diving shot Jersey upline Jonline Diving suit Atmospheric diving suit Dry suit Sladen suit Standard diving suit Rash vest Wetsuit Dive skins Hot-water suit Helmets and masks Anti-fog Diving helmet Free-flow helmet Lightweight demand helmet Orinasal mask Reclaim helmet Shallow water helmet Standard diving helmet Diving mask Band mask Full-face mask Half mask Instrumentation Bottom timer Depth gauge Dive computer Dive timer Diving watch Helium release valve Pneumofathometer Submersible pressure gauge Mobility equipment Diving bell Closed bell Wet bell Diving stage Swimfin Monofin PowerSwim Towboard Diver propulsion vehicle Advanced SEAL Delivery System Cosmos CE2F series Dry Combat Submersible Human torpedo Motorised Submersible Canoe Necker Nymph R-2 Mala-class swimmer delivery vehicle SEAL Delivery Vehicle Shallow Water Combat Submersible Siluro San Bartolomeo Wet Nellie Wet sub Safety equipment Alternative air source Octopus regulator Pony bottle Bolt snap Buddy line Dive light Diver's cutting tool Diver's knife Diver's telephone Through-water communications Diving bell Diving safety harness Emergency gas supply Bailout block Bailout bottle Lifeline Screw gate carabiner Emergency locator beacon Rescue tether Safety helmet Shark-proof cage Snoopy loop Navigation equipment Distance line Diving compass Dive reel Line marker Surface marker buoy Silt screw Underwater breathing apparatus Atmospheric diving suit Diving cylinder Burst disc Diving cylinder valve Diving helmet Reclaim helmet Diving regulator Mechanism of diving regulators Regulator malfunction Regulator freeze Single-hose regulator Twin-hose regulator Full face diving mask Open-circuit scuba Scuba set Bailout bottle Decompression cylinder Independent doubles Manifolded twin set Scuba manifold Pony bottle Scuba configuration Sidemount Sling cylinder Diving rebreathers Carbon dioxide scrubber Carleton CDBA CDLSE Cryogenic rebreather CUMA DSEA Dolphin Electro-galvanic oxygen sensor FROGS Halcyon PVR-BASC Halcyon RB80 IDA71 Interspiro DCSC KISS LAR-5 LAR-6 LAR-V LARU Porpoise Ray Siebe Gorman CDBA Siva Viper Surface-supplied diving equipment Air line Diver's umbilical Diving air compressor Gas panel Hookah Scuba replacement Sea Trek Snuba Standard diving dress Escape set Davis Submerged Escape Apparatus Momsen lung Steinke hood Submarine Escape Immersion Equipment Diving equipment manufacturers AP Diving Apeks Aqua Lung America Aqua Lung/La Spirotechnique Beuchat René Cavalero Cis-Lunar Cressi-Sub Dacor DESCO Dive Xtras Divex Diving Unlimited International Drägerwerk Fenzy Maurice Fernez Technisub Oscar Gugen Heinke HeinrichsWeikamp Johnson 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weight Launch and recovery system Wet bell Diving chamber Diving stage Recreational Dive Planner Saturation system Platforms Dive boat Canoe and kayak diving Combat Rubber Raiding Craft Liveaboard Subskimmer Diving support vessel HMS Challenger (K07) Underwater habitat Aquarius Reef Base Continental Shelf Station Two Helgoland Habitat Jules' Undersea Lodge Scott Carpenter Space Analog Station SEALAB Tektite habitat Remotely operated underwater vehicles 8A4-class ROUV ABISMO Atlantis ROV Team CURV Deep Drone Épaulard Global Explorer ROV Goldfish-class ROUV Kaikō ROV Kaşif ROUV Long-Term Mine Reconnaissance System Mini Rover ROV OpenROV ROV KIEL 6000 ROV PHOCA Scorpio ROV Sea Dragon-class ROV Seabed tractor Seafox drone Seahorse ROUV SeaPerch SJT-class ROUV T1200 Trenching Unit VideoRay UROVs Safety equipment Diver down flag Diving shot Hyperbaric lifeboat Hyperbaric stretcher Jackstay Jonline Reserve gas supply General Diving spread Air spread Saturation spread Hot water system Sonar Underwater acoustic positioning system Underwater acoustic communication Freediving Activities Aquathlon Apnoea finswimming Freediving Haenyeo Pearl hunting Ama Snorkeling Spearfishing Underwater football Underwater hockey Underwater ice hockey Underwater rugby Underwater target shooting Competitions Nordic Deep Vertical Blue Disciplines Constant weight (CWT) Constant weight without fins (CNF) Dynamic apnea (DYN) Dynamic apnea without fins (DNF) Free immersion (FIM) No-limits apnea (NLT) Static apnea (STA) Skandalopetra diving Variable weight apnea (VWT) Variable weight apnea without fins Equipment Diving mask Diving suit Hawaiian sling Polespear Snorkel (swimming) Speargun Swimfins Monofin Water polo cap Freedivers Deborah Andollo Peppo Biscarini Sara Campbell Derya Can Göçen Goran Čolak Carlos Coste Robert Croft Mandy-Rae Cruickshank Yasemin Dalkılıç Leonardo D'Imporzano Flavia Eberhard Şahika Ercümen Emma Farrell Francisco Ferreras Pierre Frolla Flavia Eberhard Mehgan Heaney-Grier Elisabeth Kristoffersen Loïc Leferme Enzo Maiorca Jacques Mayol Audrey Mestre Karol Meyer Stéphane Mifsud Alexey Molchanov Natalia Molchanova Dave Mullins Patrick Musimu Guillaume Néry Herbert Nitsch Umberto Pelizzari Annelie Pompe Michal Risian Stig Severinsen Tom Sietas Aharon Solomons Martin Štěpánek Walter Steyn Tanya Streeter William Trubridge Devrim Cenk Ulusoy Danai Varveri Alessia Zecchini Nataliia Zharkova Hazards Barotrauma Drowning Freediving blackout Deep-water blackout Shallow-water blackout Hypercapnia Hypothermia Historical Ama Octopus wrestling Swimming at the 1900 Summer Olympics – Men's underwater swimming Organisations AIDA International Scuba Schools International Australian Underwater Federation British Freediving Association Confédération Mondiale des Activités Subaquatiques Fédération Française d'Études et de Sports Sous-Marins Performance Freediving International Professional diving Occupations Ama Commercial diver Commercial offshore diver Hazmat diver Divemaster Diving instructor Diving safety officer Diving superintendent Diving supervisor Haenyeo Media diver Police diver Public safety diver Scientific diver Underwater archaeologist Military diving Army engineer diver Clearance diver Frogman List of military diving units Royal Navy ships diver Special Boat Service United States military divers U.S. ... Vandenberg HMS Ghurka Glen Strathallan SAS Good Hope Gothenburg Herzogin Cecilie Hilma Hooker Hispania HMS Hood HMAS Hobart Igara James Eagan Layne Captain Keith Tibbetts King Cruiser SMS Kronprinz Kyarra HMS Laforey USAT Liberty Louis Sheid USS LST-507 SMS Markgraf Mikhail Lermontov HMS M2 Maine Maloja HMS Maori Marguerite SS Mauna Loa USAT Meigs Mendi USCGC Mohawk Mohegan RMS Moldavia HMS Montagu MV RMS Mulheim Nagato Oceana USS Oriskany Oslofjord P29 P31 Pedernales Persier HMAS Perth SAS Pietermaritzburg Piłsudski Pool Fisher HMS Port Napier Preußen President Coolidge PS Queen Victoria Radaas Rainbow Warrior RMS Rhone Rondo Rosehill Rotorua Royal Adelaide Royal Charter Rozi HMS Safari Salem Express USS Saratoga USS Scuffle HMS Scylla HMS Sidon USS Spiegel Grove Stanegarth Stanwood Stella HMAS Swan USS Tarpon Thesis Thistlegorm Toa Maru Torrey Canyon SAS Transvaal U-40 U-352 U-1195 Um El Faroud Varvassi Walter L M Russ Washingtonian (1913) HMNZS Wellington USS Yancey Yongala Zenobia Zealandia Zingara Cave diving sites Blauhöhle Chinhoyi Caves Devil's Throat at Punta Sur Engelbrecht Cave Fossil Cave Jordbrugrotta Piccaninnie Ponds Pluragrotta Pollatoomary Sistema Ox Bel Ha Sistema Sac Actun Sistema Dos Ojos Sistema Nohoch Nah Chich Freshwater dives Dutch Springs Ewens Ponds Little Blue Lake Training sites Capernwray Dive Centre Deepspot National Diving and Activity Centre Stoney Cove Open ocean diving Blue-water diving Black-water diving Diving safety Human factors in diving equipment design Human factors in diving safety Life-support system Safety-critical system Scuba diving fatalities Diving hazards List of diving hazards and precautions Environmental Current Delta-P Entanglement hazard Overhead Silt out Wave action Equipment Freeflow Use of breathing equipment in an underwater environment Failure of diving equipment other than breathing apparatus Single point of failure Physiological Cold shock response Decompression Nitrogen narcosis Oxygen toxicity Seasickness Uncontrolled decompression Diver behaviour and competence Lack of competence Overconfidence effect Panic Task loading Trait anxiety Willful violation Consequences Barotrauma Decompression sickness Drowning Hypothermia Hypoxia Hypercapnia Hyperthermia Diving procedures Ascending and descending Emergency ascent Boat diving Canoe and kayak diving Buddy diving buddy check Decompression Decompression practice Pyle stop Ratio decompression Dive briefing Dive log Dive planning Scuba gas planning Diver communications Diving hand signals Diving line signals Diver voice communications Diver rescue Diver training Doing It Right Drift diving Gas blending for scuba diving Night diving Solo diving Water safety Risk management Checklist Hazard identification and risk assessment Hazard analysis Job safety analysis Risk assessment Risk control Hierarchy of hazard controls Incident pit Lockout–tagout Permit To Work Redundancy Safety data sheet Situation awareness Diving team Bellman Chamber operator Diver medical technician Diver's attendant Diving supervisor Diving systems technician Gas man Life support technician Stand-by diver Equipment safety Breathing gas quality Testing and inspection of diving cylinders Hydrostatic test Sustained load cracking Diving regulator Breathing performance of regulators Occupational safety and health Approaches to safety Job safety analysis Risk assessment Toolbox talk Housekeeping Association of Diving Contractors International Code of practice Contingency plan Diving regulations Emergency procedure Emergency response plan Evacuation plan Hazardous Materials Identification System Hierarchy of hazard controls Administrative controls Engineering controls Hazard elimination Hazard substitution Personal protective equipment International Marine Contractors Association Occupational hazard Biological hazard Chemical hazard Physical hazard Psychosocial hazard Occupational hygiene Exposure assessment Occupational exposure limit Workplace health surveillance Safety culture Code of practice Diving safety officer Diving superintendent Health and safety representative Operations manual Safety meeting Standard operating procedure Diving medicine Diving disorders List of signs and symptoms of diving disorders Cramp Motion sickness Surfer's ear Pressure related Alternobaric vertigo Barostriction Barotrauma Air embolism Aerosinusitis Barodontalgia Dental barotrauma Pulmonary barotrauma Compression arthralgia Decompression illness Dysbarism Oxygen Freediving blackout Hyperoxia Hypoxia Oxygen toxicity Inert gases Avascular necrosis Decompression sickness Isobaric counterdiffusion Taravana Dysbaric osteonecrosis High-pressure nervous syndrome Hydrogen narcosis Nitrogen narcosis Carbon dioxide Hypercapnia Hypocapnia Breathing gas contaminants Carbon monoxide poisoning Immersion related Asphyxia Drowning Hypothermia Immersion diuresis Instinctive drowning response Laryngospasm Salt water aspiration syndrome Swimming-induced pulmonary edema Treatment Demand valve oxygen therapy First aid Hyperbaric medicine Hyperbaric treatment schedules In-water recompression Oxygen therapy Therapeutic recompression Personnel Diving Medical Examiner Diving Medical Practitioner Diving Medical Technician Hyperbaric nursing Screening Atrial septal defect Effects of drugs on fitness to dive Fitness to dive Psychological fitness to dive Research Researchers in diving physiology and medicine Arthur J. ... Navy Diving Manual Basic Cave Diving: A Blueprint for Survival Underwater Handbook Bennett and Elliott's physiology and medicine of diving Encyclopedia of Recreational Diving The new science of skin and scuba diving Professional Diver's Handbook Basic Scuba Standards and Codes of Practice Code of Practice for Scientific Diving (UNESCO) DIN 7876 IMCA Code of Practice for Offshore Diving ISO 24801 Recreational diving services — Requirements for the training of recreational scuba divers General non-fiction The Darkness Beckons Goldfinder The Last Dive Shadow Divers The Silent World: A Story of Undersea Discovery and Adventure Research List of Divers Alert Network publications Dive guides Training and registration Diver training Competence and assessment Competency-based learning Refresher training Skill assessment Diver training standard Diving instructor Diving school Occupational diver training Commercial diver training Military diver training Public safety diver training Scientific diver training Recreational diver training Introductory diving Teaching method Muscle memory Overlearning Stress exposure training Skills Combat sidestroke Diver navigation Diver trim Ear clearing Frenzel maneuver Valsalva maneuver Finning techniques Scuba skills Buddy breathing Low impact diving Diamond Reef System Surface-supplied diving skills Underwater searches Recreational scuba certification levels Core diving skills Advanced Open Water Diver Autonomous diver CMAS* scuba diver CMAS** scuba diver Introductory diving Low Impact Diver Master Scuba Diver Open Water Diver Supervised diver Leadership skills Dive leader Divemaster Diving instructor Master Instructor Specialist skills Rescue Diver Solo diver Diver training certification and registration organisations European Underwater Federation (EUF) International Diving Regulators and Certifiers Forum (IDRCF) International Diving Schools Association (IDSA) International Marine Contractors Association (IMCA) List of diver certification organizations National Oceanic and Atmospheric Administration (NOAA) Nautical Archaeology Society Universal Referral Program World Recreational Scuba Training Council (WRSTC) Commercial diver certification authorities Australian Diver Accreditation Scheme (ADAS) Commercial diver registration in South Africa Divers Institute of Technology Health and Safety Executive (HSE) Department of Employment and Labour Commercial diving schools Divers Academy International Norwegian diver school Free-diving certification agencies AIDA International (AIDA) Confédération Mondiale des Activités Subaquatiques (CMAS) Performance Freediving International (PI) Scuba Schools International (SSI) Recreational scuba certification agencies American Canadian Underwater Certifications (ACUC) American Nitrox Divers International (ANDI) Association nationale des moniteurs de plongée (ANMP) British Sub-Aqua Club (BSAC) Comhairle Fo-Thuinn (CFT) Confédération Mondiale des Activités Subaquatiques (CMAS) Federación Española de Actividades Subacuáticas (FEDAS) Fédération Française d'Études et de Sports Sous-Marins (FFESSM) Federazione Italiana Attività Subacquee (FIAS) Global Underwater Explorers (GUE) International Association for Handicapped Divers (IAHD) International Association of Nitrox and Technical Divers (IANTD) International Diving Educators Association (IDEA) Israeli Diving Federation (TIDF) National Academy of Scuba Educators (NASE) National Association of Underwater Instructors (NAUI) Nederlandse Onderwatersport Bond (NOB) Professional Association of Diving Instructors (PADI) Professional Diving Instructors Corporation (PDIC) Sub-Aqua Association (SAA) Scuba Diving International (SDI) Scuba Educators International (SEI) Scottish Sub Aqua Club (ScotSAC) Scuba Schools International (SSI) Türkiye Sualtı Sporları Federasyonu (TSSF) United Diving Instructors (UDI) YMCA SCUBA Program Scientific diver certification authorities American Academy of Underwater Sciences (AAUS) CMAS Scientific Committee Technical certification agencies American Nitrox Divers International (ANDI) British Sub-Aqua Club (BSAC) Confédération Mondiale des Activités Subaquatiques (CMAS) Diving Science and Technology (DSAT) Federazione Italiana Attività Subacquee (FIAS) International Association of Nitrox and Technical Divers (IANTD) Professional Association of Diving Instructors (PADI) Professional Diving Instructors Corporation (PDIC) Trimix Scuba Association (TSA) Technical Extended Range (TXR) Cave diving Cave Divers Association of Australia (CDAA) Cave Diving Group (CDG) Global Underwater Explorers (GUE) National Association for Cave Diving (NACD) National Speleological Society#Cave Diving Group (CDG) National Association of Underwater Instructors (NAUI) Technical Diving International (TDI) Underwater sports Surface snorkeling Finswimming Snorkeling/breath-hold Spearfishing Underwater football Underwater hockey Australia Turkey Underwater rugby Colombia United States Underwater target shooting Breath-hold Aquathlon Apnoea finswimming Freediving Underwater ice hockey Open Circuit Scuba Immersion finswimming Sport diving Underwater cycling Underwater orienteering Underwater photography Rebreather Underwater photography Sports governing organisations and federations International AIDA International Confédération Mondiale des Activités Subaquatiques ) National AIDA Hellas Australian Underwater Federation British Freediving Association British Octopush Association British Underwater Sports Association Comhairle Fo-Thuinn Federación Española de Actividades Subacuáticas Fédération Française d'Études et de Sports Sous-Marins South African Underwater Sports Federation Türkiye Sualtı Sporları Federasyonu Underwater Society of America ) Competitions 14th CMAS Underwater Photography World Championship Underwater divers Pioneers of diving Eduard Admetlla i Lázaro Aquanaut James F. ... Barnette Victor Berge Philippe Diolé Gary Gentile Bret Gilliam Bob Halstead Trevor Jackson Steve Lewis John Mattera Rescuers Craig Challen Richard Harris Rick Stanton John Volanthen Frogmen Lionel Crabb Commercial salvors Keith Jessop Science of underwater diving Diving physics Breathing performance of regulators Buoyancy Archimedes' principle Neutral buoyancy Concentration Diffusion Molecular diffusion Force Oxygen fraction Permeation Psychrometric constant Solubility Henry's law Saturation Solution Supersaturation Surface tension Hydrophobe Surfactant Temperature Torricellian chamber Underwater acoustics Modulated ultrasound Underwater vision Snell's law Underwater computer vision Weight Apparent weight Gas laws Amontons's law Boyle's law Charles's law Combined gas law Dalton's law Gay-Lussac's law Ideal gas law Pressure Absolute pressure Ambient pressure Atmospheric pressure Gauge pressure Hydrostatic pressure Metre sea water Partial pressure Diving physiology Artificial gills Cold shock response Diving reflex Equivalent narcotic depth Lipid Maximum operating depth Metabolism Physiological response to water immersion Tissue Underwater vision Circulatory system Blood shift Patent foramen ovale Perfusion Pulmonary circulation Systemic circulation Decompression theory Decompression models: Bühlmann decompression algorithm Haldane's decompression model Reduced gradient bubble model Thalmann algorithm Thermodynamic model of decompression Varying Permeability Model Equivalent air depth Equivalent narcotic depth Oxygen window in diving decompression Physiology of decompression Respiration Blood–air barrier Breathing CO₂ retention Dead space Gas exchange Hypocapnia Respiratory exchange ratio Respiratory quotient Respiratory system Work of breathing Diving environment Classification List of diving environments by type Altitude diving Benign water diving Confined water diving Deep diving Inland diving Inshore diving Muck diving Night diving Open-water diving Black-water diving Blue-water diving Penetration diving Cave diving Ice diving Wreck diving Recreational dive sites Underwater environment Impact Environmental impact of recreational diving Low impact diving Environmental factors Algal bloom Currents: Current Longshore drift Ocean current Rip current Tidal race Undertow Upwelling Ekman transport Halocline Reef Coral reef Stratification Thermocline Tides Turbidity Wind wave Breaking wave Surf Surge Wave shoaling Other Bathysphere Defense against swimmer incursions Diver detection sonar Offshore survey Underwater domain awareness Awards and events Hans Hass Award International Scuba Diving Hall of Fame London Diving Chamber Dive Lectures NOGI Awards Deep-submergence vehicle Aluminaut DSV Alvin American submarine NR-1 Bathyscaphe Archimède FNRS-2 FNRS-3 FNRS-4 Harmony class bathyscaphe Sea Pole -class bathyscaphe Trieste II Deepsea Challenger Ictineu 3 JAGO Jiaolong Konsul -class submersible DSV Limiting Factor Russian submarine Losharik Mir Nautile Pisces -class deep submergence vehicle DSV Sea Cliff DSV Shinkai DSV Shinkai 2000 DSV Shinkai 6500 DSV Turtle DSV-5 Nemo Deep-submergence rescue vehicle LR5 LR7 MSM-1 Mystic -class deep-submergence rescue vehicle DSRV-1 Mystic DSRV-2 Avalon NATO Submarine Rescue System Priz -class deep-submergence rescue vehicle Russian deep submergence rescue vehicle AS-28 Russian submarine AS-34 ASRV Remora SRV-300 Submarine Rescue Diving Recompression System Type 7103 DSRV URF (Swedish Navy) Special interest groups Artificial Reef Society of British Columbia CMAS Europe Coral Reef Alliance Diving Equipment and Marketing Association Divers Alert Network Green Fins Historical Diving Society Karst Underwater Research Nautical Archaeology Program Nautical Archaeology Society Naval Air Command Sub Aqua Club Project AWARE Reef Check Reef Life Survey Rubicon Foundation Save Ontario Shipwrecks SeaKeys Sea Research Society Society for Underwater Historical Research Society for Underwater Technology Underwater Archaeology Branch, Naval History & Heritage Command Submarine escape and rescue Escape trunk International Submarine Escape and Rescue Liaison Office McCann Rescue Chamber Submarine Escape and Rescue system (Royal Swedish Navy) Submarine escape training facility Submarine Escape Training Facility (Australia) Submarine rescue ship Neutral buoyancy facilities for Astronaut training Neutral Buoyancy Laboratory Neutral buoyancy pool Neutral buoyancy simulation as a training aid Neutral Buoyancy Simulator Space Systems Laboratory Yuri Gagarin Cosmonaut Training Center Other Nautilus Productions Category Commons Glossary Indexes: dive sites divers diving Outline Portal
    SCN4A, ANXA11, SOD1, TAF1, TSPYL1, VCP, TAF15, SQSTM1, VAPB, MATR3, FIG4, OPTN, ANG, UNC13A, TARDBP, CHMP2B, SRPX2, TBK1, UBQLN2, TREM2, GLT8D1, UBE3B, C9orf72, PPARGC1A, ATXN2, PRPH, GLE1, BTD, CFAP410, CCNF, DAO, DCTN1, EPHA4, ERBB4, FUS, GABRG2, GRIN2A, PON3, HNRNPA1, LAMA3, LAMB3, LAMC2, NEFH, NEK1, PFN1, PON1, PON2, CHCHD10
  • Restless Legs Syndrome Mayo_clinic
    Worsening of symptoms in the evening. Symptoms occur mainly at night. Nighttime leg twitching. RLS may be associated with another, more common condition called periodic limb movement of sleep, which causes the legs to twitch and kick, possibly throughout the night, while you sleep. ... Your symptoms are partially or temporarily relieved by activity, such as walking or stretching. Your symptoms are worse at night. Symptoms can't be explained solely by another medical or behavioral condition. ... This may involve an overnight stay and a study at a sleep clinic if another sleep disorder such as sleep apnea is suspected. However, a diagnosis of RLS usually doesn't require a sleep study. ... These drugs help you sleep better at night, but they don't eliminate the leg sensations, and they may cause daytime drowsiness. ... Do your symptoms start while you're sitting or lying down? Are your symptoms worse at night? Does movement make you feel better?
    BTBD9, MEIS1, PTPRD, TF, POMC, DRD3, MAP2K5, SNCA, PRKN, MFN2, LRRK2, PARK7, FTL, HTRA2, VPS13C, DNAJC6, ATXN7, LINC02086, PINK1, UCHL1, RLS1, CASC16, PODXL, MYT1, LINC02520, LINC01478, CCDC148, SKOR1, HMOX1, TOX3, DRD2, VDR, MAOA, RLS3, CHM, FXYD1, TH, CHMP2B, SLC11A2, ATXN1, HAMP, GABRR3, RLS4, RLS6, NTS, ADH1B, HMOX2, CRP, GABRA4, FXN, EEF1A2, DMRT1, KNG1, IL1B, HFE, MPZ, MAOB, NOS1, ATXN3, ZC4H2, MIXL1, REEP1, AVP, PCDHA3, MOCOS, FAT2, GABRR2, NANS, SLC25A37, ATL1, PYCARD, GCH1, FMR1, C3, TRAPPC6B, CAD, TMPRSS6, DRD4, GLO1, C9orf72, DBP, MIR122, LINC00423, MIR330, RLS2, CPT1B, CHKB, RLS5, KCTD18, NPAS2, SPATS2L, MCF2L, NKX2-1, TFRC, IL17A, TRA, AFP, SLC6A3, SLC1A2, L1CAM, ATXN2, LRP2, TSPAN31, REN, LY6E, SMCP, SERPINA1, TNF, TYMS, IGLC2, SCAF11, CNTN3, HNMT, ZEB2, IGHA1, LITAF, SLC9A3R2, APLN, UTRN, RNMT, GEMIN2, ATRN, FGF23, NR4A3, IGKC, TBP
    • Restless Legs Syndrome Wikipedia
      "Variability over the course of the day-night cycle, with symptoms worse in the evening and early in the night." Some experience RLS only at bedtime, while others experience it throughout the day and night. Most people experience the worst symptoms in the evening and the least in the morning. ... It improves or disappears (at least temporarily) with activity. It worsens in the evening or night. These symptoms are not caused by any medical or behavioral condition. These symptoms are not essential, like the ones above, but occur commonly in RLS patients: [1] [55] genetic component or family history with RLS good response to dopaminergic therapy periodic leg movements during day or sleep most strongly affected are people who are middle-aged or older other sleep disturbances are experienced decreased iron stores can be a risk factor and should be assessed According to the International Classification of Sleep Disorders (ICSD-3), the main symptoms have to be associated with a sleep disturbance or impairment in order to support RLS diagnosis. [56] As stated by this classification, RLS symptoms should begin or worsen when being inactive, be relieved when moving, should happen exclusively or mostly in the evening and at night, not be triggered by other medical or behavioral conditions, and should impair one's quality of life. [56] [57] Generally, both legs are affected, but in some cases there is an asymmetry. ... "A questionnaire study of 138 patients with restless legs syndrome: The 'Night-Walkers' survey". Neurology . 46 (1): 92–5. doi : 10.1212/WNL.46.1.92 .
  • Tonsillitis Wikipedia
    "Circulating phospholipase-A2 activity in obstructive sleep apnea and recurrent tonsillitis". Int J Pediatr Otorhinolaryngol . 76 (4): 471–4. doi : 10.1016/j.ijporl.2011.12.026 . PMID 22297210 . ^ van Kempen MJ, Rijkers GT, Van Cauwenberge PB (May 2000). "The immune response in adenoids and tonsils". Int. Arch. Allergy Immunol. ... "Tissue fatty acid composition in obstructive sleep apnea and recurrent tonsillitis". Int J Pediatr Otorhinolaryngol . 77 (6): 1008–12. doi : 10.1016/j.ijporl.2013.03.033 . ... Wetmore RF (2007). "Tonsils and adenoids". In Kliegman RM, Behrman RE, Jenson HB, Stanton BF (eds.). ... Classification D ICD - 10 : J03 , J35.0 ICD - 9-CM : 463 MeSH : D014069 DiseasesDB : 13165 External resources MedlinePlus : 001043 eMedicine : article/871977 Patient UK : Tonsillitis v t e Diseases of the respiratory system Upper RT (including URTIs , common cold ) Head sinuses Sinusitis nose Rhinitis Vasomotor rhinitis Atrophic rhinitis Hay fever Nasal polyp Rhinorrhea nasal septum Nasal septum deviation Nasal septum perforation Nasal septal hematoma tonsil Tonsillitis Adenoid hypertrophy Peritonsillar abscess Neck pharynx Pharyngitis Strep throat Laryngopharyngeal reflux (LPR) Retropharyngeal abscess larynx Croup Laryngomalacia Laryngeal cyst Laryngitis Laryngopharyngeal reflux (LPR) Laryngospasm vocal cords Laryngopharyngeal reflux (LPR) Vocal fold nodule Vocal fold paresis Vocal cord dysfunction epiglottis Epiglottitis trachea Tracheitis Laryngotracheal stenosis Lower RT / lung disease (including LRTIs ) Bronchial / obstructive acute Acute bronchitis chronic COPD Chronic bronchitis Acute exacerbation of COPD ) Asthma ( Status asthmaticus Aspirin-induced Exercise-induced Bronchiectasis Cystic fibrosis unspecified Bronchitis Bronchiolitis Bronchiolitis obliterans Diffuse panbronchiolitis Interstitial / restrictive ( fibrosis ) External agents/ occupational lung disease Pneumoconiosis Aluminosis Asbestosis Baritosis Bauxite fibrosis Berylliosis Caplan's syndrome Chalicosis Coalworker's pneumoconiosis Siderosis Silicosis Talcosis Byssinosis Hypersensitivity pneumonitis Bagassosis Bird fancier's lung Farmer's lung Lycoperdonosis Other ARDS Combined pulmonary fibrosis and emphysema Pulmonary edema Löffler's syndrome / Eosinophilic pneumonia Respiratory hypersensitivity Allergic bronchopulmonary aspergillosis Hamman-Rich syndrome Idiopathic pulmonary fibrosis Sarcoidosis Vaping-associated pulmonary injury Obstructive / Restrictive Pneumonia / pneumonitis By pathogen Viral Bacterial Pneumococcal Klebsiella Atypical bacterial Mycoplasma Legionnaires' disease Chlamydiae Fungal Pneumocystis Parasitic noninfectious Chemical / Mendelson's syndrome Aspiration / Lipid By vector/route Community-acquired Healthcare-associated Hospital-acquired By distribution Broncho- Lobar IIP UIP DIP BOOP-COP NSIP RB Other Atelectasis circulatory Pulmonary hypertension Pulmonary embolism Lung abscess Pleural cavity / mediastinum Pleural disease Pleuritis/pleurisy Pneumothorax / Hemopneumothorax Pleural effusion Hemothorax Hydrothorax Chylothorax Empyema/pyothorax Malignant Fibrothorax Mediastinal disease Mediastinitis Mediastinal emphysema Other/general Respiratory failure Influenza Common cold SARS Coronavirus disease 2019 Idiopathic pulmonary haemosiderosis Pulmonary alveolar proteinosis Authority control NDL : 00563120
    GALNS, PAGR1, GAST, MBL3P, VDR, IFNG, IL1B, MBL2, DEFB1, RXRB, TRBV20OR9-2, S100A7, CCL20, CCL24, SKP1, SOD2, BCL2, TNFSF13, TLR4, PRCP, PDLIM7, ANP32B, CCL27, PART1, TLR9, AICDA, RNASE2, LTF, MTHFR, CCNB1, CDKN2A, EGFR, FANCD2, FCN2, GEM, GPX1, HIF1A, HLA-B, HLA-C, IGHG3, IL6, CXCL8, IL10, KIR2DS1, KIR3DL1, KIR3DL2, LTA, FDCSP
    • Tonsillitis Mayo_clinic
      Complications Inflammation or swelling of the tonsils from frequent or ongoing (chronic) tonsillitis can cause complications such as: Disrupted breathing during sleep (obstructive sleep apnea) Infection that spreads deep into surrounding tissue (tonsillar cellulitis) Infection that results in a collection of pus behind a tonsil (peritonsillar abscess) Strep infection If tonsillitis caused by group A streptococcus or another strain of streptococcal bacteria isn't treated or if antibiotic treatment is incomplete, your child has an increased risk of rare disorders such as: Rheumatic fever, a serious inflammatory condition that can affect the heart, joints, nervous system and skin Complications of scarlet fever, a streptococcal infection characterized by a prominent rash Inflammation of the kidney (poststreptococcal glomerulonephritis) Poststreptococcal reactive arthritis, a condition that causes inflammation of the joints Prevention The germs that cause viral and bacterial tonsillitis are contagious. ... Frequent tonsillitis is generally defined as: At least seven episodes in the preceding year At least five episodes a year in the past two years At least three episodes a year in the past three years A tonsillectomy may also be performed if tonsillitis results in difficult-to-manage complications, such as: Obstructive sleep apnea Breathing difficulty Swallowing difficulty, especially meats and other chunky foods An abscess that doesn't improve with antibiotic treatment A tonsillectomy is usually done as an outpatient procedure, unless your child is very young, has a complex medical condition or if complications arise during surgery.
  • Apert Syndrome Gene_reviews
    If airway obstruction is present, temporizing measures may be required. Treatment of sleep apnea by surgical intervention and/or supplemental oxygen via nasal cannula may be required. ... Agents/circumstances to avoid: Contact sports and activities that involve neck hyperflexion or extension for those with cervical spine anomalies; factors that potentiate hearing loss; use of CPAP/BiPAP for long-term treatment of sleep apnea. Pregnancy management: For affected pregnant women: monitoring for signs and symptoms of worsening obstructive sleep apnea and anethesia evaluation prior to initiation of labor to identify any multilevel airway anomalies or vertebral anomalies that would result in additional risk with certain types of anesthesia; fiberoptic intubation could be required. ... Avoid use of CPAP/BiPAP for long-term treatment of sleep apnea when possible because pressure on midface exacerbates midfacial retrusion. Supplemental oxygen via nasal cannula is sometimes beneficial. Reducing sleep apnea & improving sleep quality has the potential to improve learning, cognition, & behavior. ... Use of CPAP/BiPAP for long-term treatment of sleep apnea should be avoided when possible because pressure on the midface will exacerbate midfacial retrusion.
    FGFR2, TWIST1, RAB18, TBC1D20, FGF2, FGFR3, FGF10, FGFR1, FN1, FGF8, FGF13, BMP2, PIN1, MAPK8, RET, STAT3, ERF, FGF19, COL2A1, CCND1
    • Apert Syndrome Medlineplus
      Apert syndrome is a genetic disorder characterized by skeletal abnormalities. A key feature of Apert syndrome is the premature closure of the bones of the skull (craniosynostosis). This early fusion prevents the skull from growing normally and affects the shape of the head and face. In addition, a varied number of fingers and toes are fused together (syndactyly). Craniosynostosis causes many of the characteristic facial features of Apert syndrome.
    • Apert Syndrome Orphanet
      A frequent form of acrocephalosyndactyly, a group of inherited congenital malformation disorders, characterized by craniosynostosis, midface hypoplasia, and finger and toe anomalies and/or syndactyly. Epidemiology The estimated incidence of Apert syndrome is reported to be 1/100,000 to 1/160,000 live births. Clinical description Patients generally have extensive structural and functional impairments related to cranial and limb deformities. Craniosynostosis can lead to acrobrachycephaly or turribrachycephaly with delayed closure of fontanels and a possible impact on brain growth and neurological development. Macrocephaly is also found. Limb malformations mainly consist of soft tissue and bony syndactyly of fingers and toes (involving variable numbers of digits), occasional rhizomelic shortening, and elbow ankylosis, with functional impairments and restriction of mobility.
  • Maroteaux–lamy Syndrome Wikipedia
    It may be necessary to remove the tonsils and/or adenoids. Severe tracheomalacia may require surgery. ... Aggressive management of airway secretions is necessary as well. Sleep apnea may be treated with a CPAP or BPAP device. [5] Prognosis [ edit ] A slowly-progressing female patient in her 20s, showing few physical abnormalities The life expectancy of individuals with MPS VI varies depending on the severity of symptoms.
    ARSB, ADAMTS5, GUSB, ALAS2, IDS, ACP2, ACP5, ARSA, CD1D, CD34, PGRMC1
    • Mucopolysaccharidosis, Type Vi Omim
      Respiratory problems were indicated by difficult intubation and problems with sleep apnea. Neufeld and Muenzer (1995) classified patients with MPS VI into severe, intermediate, or mild forms. ... Herskhovitz et al. (1999) described the results of bone marrow transplantation (BMT) in 4 patients with MPS VI, 3 of whom underwent BMT due to cardiomyopathy and 1 for severe obstructive sleep apnea. During a follow-up period ranging between 1 and 9 years, the facial features became less coarse in all patients and cardiac manifestations improved or remained stable.
    • Mucopolysaccharidosis Type Vi Medlineplus
      The airway may become narrow in some people with MPS VI, leading to frequent upper respiratory infections and short pauses in breathing during sleep (sleep apnea). The clear covering of the eye (cornea ) typically becomes cloudy, which can cause significant vision loss.
    • Mucopolysaccharidosis Type 6 Orphanet
      Other clinical findings may include cardiac valve disease, reduced pulmonary function, hepatosplenomegaly, sinusitis, otitis media, hearing loss, sleep apnea, corneal clouding, carpal tunnel disease, and inguinal or umbilical hernia.
  • Confusional Arousals Wikipedia
    The altered state of consciousness may be explained by a hypersynchronous delta activity (see delta wave ) in network involving the frontoparietal cortices (suggesting to be "asleep"), and higher frequency activities in sensorimotor, orbitofrontal, and temporal lateral cortices (suggesting an "awakening"). [6] [7] Sleep-related violence and abnormal sexual behaviours [ edit ] Confusional arousals have often been linked to sleep-related violence (self-injury or injury to the bed partner). [8] [9] [10] [11] The latter highlights important medical and legal issues when such behaviours are suspected and purported to have caused a criminal offense. [12] The first documented case of homicide as a result of confusional arousal was reported in medieval times by the case of the Silesian woodcutter Bernard Schedmaizig. [13] Sleep-related abnormal sexual behaviours (also called sexsomnia or sleep sex ) are mainly classified as confusional arousals and more rarely associated to sleepwalking (also known as somnambulism). [12] Even if sleep-related violence may occur during an episode of confusional arousal, it remains extremely rare and there are no specific predisposition to aggression during these episodes. [8] Distinction between sleepwalking and night terrors [ edit ] Violent behaviours in confusional arousals slightly differ from those in sleepwalking or night terrors. [8] Above all, during an episode of confusional arousal the patient never leaves the bed unlike sleepwalking. ... Unlike confusional arousals and sleep walking, patients experiencing night terrors seem to react to some type of frightening image. ... NREM parasomnias (or disorders of arousal) also include sleep terrors (see night terror ) and sleepwalking . Confusional arousals are characterised by more or less complex movements without leaving bed with whimpering, sitting up in bed and some articulation without walking or terror. [14] [15] In comparison of other arousal parasomnias the age onset of sleep walking is generally between 5 and 10 years whereas confusional arousals and sleep terror may occur 3 years earlier. ... According to studies, [2] [21] [22] they are shift work, hypnagogic hallucinations (also known as hypnagogia ), excessive daytime sleepiness, insomnia and hypersomnia disorder, circadian rhythm sleep disorder , restless legs syndrome , obstructive sleep apnea syndrome (OSAS), bipolar disorder , daily smoking, and age of 15–24 years. ... G.; Guilleminault, C.; Ohayon, M. M. (April 1999). "Night terrors, sleepwalking, and confusional arousals in the general population: their frequency and relationship to other sleep and mental disorders".
  • Glaucoma-Sleep Apnea Syndrome Orphanet
    Glaucoma-sleep apnea syndrome is characterized by sleep apnoea associated with glaucoma.
    • Glaucoma And Sleep Apnea Omim
      Two other surviving brothers had only sleep apnea with no glaucoma. In those who had recordings, episodes of sleep apnea tended to occur and to be more prolonged in rapid-eye-movement sleep.
  • Pitt-Hopkins Syndrome Gene_reviews
    Sleep disturbance in childhood is reported in fewer than half of affected individuals [Whalen et al 2012] and includes difficulty falling asleep, problems sleeping through the night, and night terrors [de Winter et al 2016]. ... Episodic hyperventilation often followed by breath-holding/apnea while awake are reported in 40%-60% of individuals [Whalen et al 2012, de Winter et al 2016, Goodspeed et al 2018]. ... However, in most affected individuals breathing abnormalities persist to some degree, though too few adults have been described to make conclusive statements about frequency or severity. Breath-holding/apnea episodes are not typically related to seizure activity [Maini et al 2012]. ... The breathing abnormality in PTHS does not appear to be a manifestation of seizure activity [Maini et al 2012], though in this study, 7/38 individuals with seizures had apnea or hyperventilation shortly before their seizures. ... Polysomnography may be indicated if there is a history of episodic apnea, especially when associated with cyanosis (typically alternating with episodes of hyperventilation).
    TCF4, NRXN1, CNTNAP2, NEUROD1, ATR, FOXG1, HTC2, MECP2, PTEN
    • Pitt-Hopkins Syndrome Omim
      Description The Pitt-Hopkins syndrome is characterized by mental retardation, wide mouth and distinctive facial features, and intermittent hyperventilation followed by apnea (Zweier et al., 2007). See also Pitt-Hopkins-like syndrome-1 (610042), caused by mutation in the CNTNAP2 gene (604569) on chromosome 7q35, and Pitt-Hopkins-like syndrome-2 (600565), caused by mutation in the NRXN1 gene (600565) on chromosome 2p16.3. ... He overbreathed at up to 120 breaths per minute for 1 to 2 minutes and then had a period of apnea for up to 2 minutes, during the latter part of which he became cyanosed until a new episode of overbreathing terminated the cyanosis.
    • Pitt-Hopkins Syndrome Gard
      Pitt-Hopkins syndrome (PTHS) is a genetic syndrome that causes developmental delays, moderate to severe intellectual disability, behavioral differences, distinctive facial features, and breathing problems such as episodes of rapid breathing ( hyperventilation ) and breath-holding. Other features may include symptoms of autism spectrum disorder, sleep disturbances, seizures, constipation, nearsightedness, and minor skeletal abnormalities. PTHS is caused by a mutation in the TCF4 gene, or by a loss (deletion) of the part of chromosome 18 that contains the TCF4 gene. Inheritance is autosomal dominant, but PTHS typically is not inherited from a parent, occurring sporadically due to a new mutation in people with no family history of PTHS. The diagnosis may be suspected based on signs and symptoms and can be confirmed with genetic testing.
    • Pitt–hopkins Syndrome Wikipedia
      Pitt–Hopkins syndrome Boy with Pitt–Hopkins syndrome showing the characteristic facial features Specialty Psychiatry , Medical genetics Pitt–Hopkins syndrome ( PTHS ) is a rare genetic disorder characterized by developmental delay , epilepsy , distinctive facial features , and possible intermittent hyperventilation followed by apnea . [1] As more is learned about Pitt–Hopkins, the developmental spectrum of the disorder is widening, and can also include difficulties with anxiety , autism , [2] ADHD , and sensory disorders. ... Hyperventilation may occur and is sometimes followed by apnea and cyanosis . Constipation is common.
    • Pitt-Hopkins Syndrome Orphanet
      Typically, the bouts of hyperventilation come without eliciting factor, have a duration of 2-5 minutes, and are often followed by apnea. Hyperventilation and apnea may also occur independently.
    • Pitt-Hopkins Syndrome Medlineplus
      Breathing problems in individuals with Pitt-Hopkins syndrome are characterized by episodes of rapid breathing (hyperventilation) followed by periods in which breathing slows or stops (apnea). These episodes can cause a lack of oxygen in the blood, leading to a bluish appearance of the skin or lips (cyanosis). ... The breathing problems occur only when the person is awake and typically first appear in mid-childhood, but they can begin as early as infancy. Episodes of hyperventilation and apnea can be triggered by emotions such as excitement or anxiety or by extreme tiredness (fatigue).
  • Shift Work Sleep Disorder Wikipedia
    It is believed that the reduction in firing in the SCN stimulates sleep. [30] While day-active individuals produce melatonin at night, night shift workers' production of melatonin is suppressed at night due to light exposure. [31] Circadian misalignment [ edit ] Circadian misalignment plays a major role in shift work sleep disorder. ... A nap before starting a night shift is a logical prophylactic measure. ... "Dark goggles and bright light improve circadian rhythm adaptation to night-shift work" . Sleep . 17 (6): 535–43. doi : 10.1093/sleep/17.6.535 . ... "The effects of caffeine on simulated night-shift work and subsequent daytime sleep" . ... "Sleepiness/alertness on a simulated night shift following sleep at home with triazolam" .
    AANAT, CRY1, NFIL3, RORC, BHLHE40
  • Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic Omim
    He also had frequent attacks of cyanosis and apnea. At age 8 weeks, he showed general retardation and atrophy of the optic nerve. ... He had no signs of infection, but had been very active the night before. Lactate, pyruvate, and ammonia were normal, free fatty acids were elevated, and GPT was slightly elevated. ... INHERITANCE - Autosomal recessive HEAD & NECK Eyes - Optic nerve atrophy RESPIRATORY - Apnea, episodic ABDOMEN Liver - Enlarged liver - Fatty infiltration - Portal inflammation, mild to moderate Portal fibrosis, mild - Patchy to diffuse macrovesicular steatosis - Acute liver failure, transient (in 1 patient) SKIN, NAILS, & HAIR Skin - Cyanosis NEUROLOGIC Central Nervous System - Seizures (in some patients) - Hepatic encephalopathy (in 1 patient) METABOLIC FEATURES - Cytosolic phosphoenolpyruvate carboxykinase deficiency - Impaired gluconeogenesis - Fasting hypoglycemia - Lactic acidemia - Normal to elevated blood ammonia - Elevated blood alanine aminotransferase - Normal to high plasma glutamine - Normal to low plasma citrulline - Normal to low plasma arginine - Ketonuria - Elevated urine lactate - Prominent tricarboxylic acid cycle metabolites in urine (particularly fumarate) MISCELLANEOUS - Onset in infancy ▲ Close
    PCK1, PCK2
    • Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial Omim
      Clinical Features In 2 unrelated children, Hommes et al. (1976) observed hypoglycemia and liver impairment, with deficiency of PEPCK (614095) in liver tissue taken immediately after death. Massive fatty deposition in liver and kidneys was found at autopsy. Fiser et al. (1974) also observed hypoglycemia caused by deficiency of PEPCK. Other enzymatic causes of hypoglycemia include glucose-6-phosphatase deficiency (232200), fructose-1,6-diphosphatase deficiency (229700), and pyruvate carboxylase deficiency (266150). Robinson et al. (1980) studied skin fibroblast cultures from 40 pediatric cases of lactic acidosis. They found one case in which mitochondrial activity of phosphoenolpyruvate carboxykinase was 6% of normal.
    • Phosphoenolpyruvate Carboxykinase Deficiency Orphanet
      Phosphoenolpyruvate carboxykinase (PEPCK) deficiency is a gluconeogenesis disorder that results from impairment in the enzyme PEPCK, and comprising cytosolic (PEPCK1) and mitochondrial (PEPCK2) forms of enzyme deficiency. Onset of symptoms is neonatal or a few months after birth and includes hypoglycemia associated with acute episodes of severe lactic acidosis, progressive neurological deterioration, severe liver failure, renal tubular acidosis and Fanconi syndrome. Patients also present progressive multisystem damage with failure to thrive, muscular weakness and hypotonia, developmental delay with seizures, spasticity, lethargy, microcephaly and cardiomyopathy. To date, there is no conclusive evidence of the existence of an isolated form of this disorder.
    • Pepck 1 Deficiency Gard
      PEPCK1 deficiency is a rare inborn error of metabolism disorder , characterized by the deficiency of the enzyme PEPCK1, one of the enzymes needed for gluconeogenesis , the process by which organisms produce sugars (namely glucose) from non-carbohydrate precursors (such as amino acids). The symptoms described in the few cases reported in the medical literature suggest that there may be variation in the severity of the symptoms ranging from severe early-onset cases, to milder late-onset presentations. In severe cases symptoms may include persistent and very low levels of blood's sugar in newborns (neonatal hypoglycemia), failure to thrive, build-up of lactic acid in the blood ( lactic acidosis ), liver enlargement (hepatomegaly) and liver failure leading to neurological degeneration. Milder cases present during childhood with fewer and less serious liver problems. Infections and fasting may trigger the symptoms. PEPCK1 deficiency inheritance is autosomal recessive.
  • Jet Lag Wikipedia
    Cognitive effects include poorer performance on mental tasks and concentration ; dizziness, nausea , insomnia , confusion, anxiety , increased fatigue , headaches , and irritability ; and problems with digestion, including indigestion , changes in the frequency of defecation and consistency of faeces , and reduced interest in and enjoyment of food. [2] The symptoms are caused by a circadian rhythm that is out of sync with the day-night cycle of the destination, [3] as well as the possibility of internal desynchronisation. ... Travel fatigue can occur without crossing time zones, and it often disappears after one day accompanied by a night of good quality sleep. [3] Cause [ edit ] Jet lag is a chronobiological problem, [6] similar to issues often induced by shift work and the circadian rhythm sleep disorders. ... Equally important, the necessary exposure to light to realign the body clock does not tie in with the day/night cycle at the destination. [3] Travelling east by six to nine time zones causes the biggest problems, as it is desirable to avoid light in the mornings. ... Management when travelling west [ edit ] Travelling west causes fewer problems than travelling east, and it is usually sufficient to seek exposure to light during the day and avoid it at night. [3] The advice is to prepare by having late sleep times the days before, and to travel daytime (not so early that early wakeup is needed) and to sleep some on board in order to be less tired at arrival and during ground transfer. ... External links [ edit ] Classification D ICD - 10 : G47.25 ICD - 9-CM : 307.45 , 780.50 327.35 MeSH : D021081 DiseasesDB : 7045 v t e Sleep and sleep disorders Stages of sleep cycles Rapid eye movement (REM) Non-rapid eye movement Slow-wave Brain waves Alpha wave Beta wave Delta wave Gamma wave K-complex Mu rhythm PGO waves Sensorimotor rhythm Sleep spindle Theta wave Sleep disorders Dyssomnia Excessive daytime sleepiness Hypersomnia Insomnia Kleine–Levin syndrome Narcolepsy Night eating syndrome Nocturia Sleep apnea Catathrenia Central hypoventilation syndrome Obesity hypoventilation syndrome Obstructive sleep apnea Periodic breathing Sleep state misperception Circadian rhythm disorders Advanced sleep phase disorder Cyclic alternating pattern Delayed sleep phase disorder Irregular sleep–wake rhythm Jet lag Non-24-hour sleep–wake disorder Shift work sleep disorder Parasomnia Bruxism Nightmare disorder Night terror Periodic limb movement disorder Rapid eye movement sleep behavior disorder Sleepwalking Somniloquy Benign phenomena Dreams Exploding head syndrome Hypnic jerk Hypnagogia / Sleep onset Hypnopompic state Sleep paralysis Sleep inertia Somnolence Nocturnal clitoral tumescence Nocturnal penile tumescence Nocturnal emission Treatment Sleep diary Sleep hygiene Sleep induction Hypnosis Lullaby Somnology Polysomnography Other Sleep medicine Behavioral sleep medicine Sleep study Daily life Bed Bunk bed Daybed Four-poster bed Futon Hammock Mattress Sleeping bag Bed bug Bedding Bedroom Bedtime Bedtime story Bedtime toy Biphasic and polyphasic sleep Chronotype Dream diary Microsleep Mouth breathing Nap Nightwear Power nap Second wind Siesta Sleep and creativity Sleep and learning Sleep deprivation / Sleep debt Sleeping while on duty Sleepover Snoring
    CLOCK, ARNTL, PER2, SREBF1, DELEC1, XPR1, PER3, BHLHE40, SCD, AVP, ATXN2, PER1, NOS2, COX1, HIF1A, CRY1, TRARG1
  • Binge Eating Wikipedia
    With obesity comes a myriad of health complications: sleep apnea , cancer , heart disease , high blood pressure , type 2 diabetes , arthritis . [6] Effects [ edit ] Typically the eating is done rapidly and a person will feel emotionally numb and unable to stop eating. [7] Most people who have eating binges try to hide this behavior from others, and often feel ashamed about being overweight or depressed about their overeating. ... He also reported that some of these cases unhealthy eating habits were seen during a time period he called “night eating”. After this report, the terminology of “Binge Eating” caught on for diagnosing the episodes of infrequent eating of large amounts of food, whether or not the episode is connected with night eating. [11] 1987: The APA's DSM [ edit ] The American Psychiatric Association (APA) mentioned and listed Binge Eating under the listed criteria and features of Bulimia in the Diagnostic and Statistical Manual of Mental Disorders (DSM) - 3 in 1987.
    CNR1, DRD1, DRD2, DRD4
    • Binge-Eating Disorder Mayo_clinic
      Overview Binge-eating disorder is a serious eating disorder in which you frequently consume unusually large amounts of food and feel unable to stop eating. Almost everyone overeats on occasion, such as having seconds or thirds of a holiday meal. But for some people, excessive overeating that feels out of control and becomes a regular occurrence crosses the line to binge-eating disorder. When you have binge-eating disorder, you may be embarrassed about overeating and vow to stop. But you feel such a compulsion that you can't resist the urges and continue binge eating.
    • Binge Eating Disorder Wikipedia
      Precisely defining binge eating can be problematic, [2] however binge eating episodes in BED are generally described as having the following potential features: Eating much faster than normal, [7] perhaps in a short space of time [8] Eating until feeling uncomfortably full [7] Eating a large amount when not hungry [7] Subjective loss of control over how much or what is eaten [9] Binges may be planned in advance, [7] involving the purchase of special binge foods, [7] and the allocation of specific time for binging, sometimes at night Eating alone or secretly due to embarrassment over the amount of food consumed [7] There may be a dazed mental state during the binge [7] Not being able to remember what was eaten after the binge [7] Feelings of guilt, shame or disgust following a food binge [7] [9] In contrast to bulimia nervosa, binge eating episodes are not regularly followed by activities intended to prevent weight gain, [2] such as self-induced vomiting, laxative or enema misuse, or strenuous exercise. [9] BED is characterized more by overeating than dietary restriction and over concern about body shape. [2] Obesity is common in persons with BED, [2] as are depressive features, [2] low self-esteem, stress and boredom. [8] Causes [ edit ] As with other eating disorders, binge eating is an "expressive disorder"—a disorder that is an expression of deeper psychological problems. [3] People who have binge eating disorder have been found to have higher weight bias internalization, which includes low self-esteem, unhealthy eating patterns, and general body dissatisfaction. [10] Binge eating disorder commonly develops as a result or side effect of depression, as it is common for people to turn to comfort foods when they are feeling down. [11] There was resistance to give binge eating disorder the status of a fully fledged eating disorder because many perceived binge eating disorder to be caused by individual choices. [5] Previous research has focused on the relationship between body image and eating disorders, and concludes that disordered eating might be linked to rigid dieting practices. [12] In the majority of cases of anorexia, extreme and inflexible restriction of dietary intake leads at some point to the development of binge eating, weight regain, bulimia nervosa, or a mixed form of eating disorder not otherwise specified. ... Mental and emotional consequences of binge eating disorder include social weight stigma and emotional loss of control. [43] Up to 70% of individuals with BED may also be obese, [8] and therefore obesity-associated morbidities such as high blood pressure [8] and coronary artery disease [8] type 2 diabetes mellitus gastrointestinal issues (e.g., gallbladder disease), high cholesterol levels , musculoskeletal problems and obstructive sleep apnea [32] [34] [44] may also be present. ... However, the prevalence of eating disorders is increasing in other non-Western countries. [51] Though the research on binge eating disorders tends to be concentrated in North America, the disorder occurs across cultures. [52] In the USA, BED is present in 0.8% of male adults and 1.6% of female adults in a given year. [28] The prevalence of BED is lower in Nordic countries compared to Europe in a study that included Finland, Sweden, Norway, and Iceland. [51] The point prevalence ranged from 0.4 to 1.5 percent and the lifetime prevalence ranged from 0.7 to 5.8 percent for BED in women. [51] In a study that included Argentina, Brazil, Chile, Colombia, Mexico, and Venezuela, the point prevalence for BED was 3.53 percent. [53] Therefore, this particular study found that the prevalence for BED is higher in these Latin American countries compared to Western countries. [53] The prevalence of BED in Europe ranges from <1 to 4 percent. [54] Co-morbidities [ edit ] BED is co-morbid with diabetes, hypertension, previous stroke, and heart disease in some individuals. [46] In people who have obsessive-compulsive disorder or bipolar I or II disorders, BED lifetime prevalence was found to be higher. [46] Additionally, 30 to 40 percent of individuals seeking treatment for weight-loss can be diagnosed with binge eating disorder. [32] Underreporting in Men [ edit ] Eating disorders are oftentimes underreported in men. [51] Underreporting could be a result of measurement bias due to how eating disorders are defined. [51] The current definition for eating disorders focuses on thinness. [51] However, eating disorders in men tend to center on muscularity and would therefore warrant a need for a different measurement definition. [51] Further research should focus on including more men in samples since previous research has focused primarily on women. [51] History [ edit ] The disorder was first described in 1959 by psychiatrist and researcher Albert Stunkard as " night eating syndrome " (NES). [55] The term "binge eating" was coined to describe the same bingeing-type eating behavior but without the exclusive nocturnal component. [56] There is generally less research on binge eating disorder in comparison to anorexia nervosa and bulimia nervosa. [5] See also [ edit ] Prader–Willi syndrome References [ edit ] ^ Agüera, Zaida; Lozano-Madrid, María; Mallorquí-Bagué, Núria; Jiménez-Murcia, Susana; Menchón, José M.; Fernández-Aranda, Fernando (28 April 2020).
  • Muscular Dystrophy Mayo_clinic
    People with muscular dystrophy might eventually need to use a breathing assistance device (ventilator), initially at night but possibly also during the day. ... As respiratory muscles weaken, a sleep apnea device might help improve oxygen delivery during the night.
    LAMA2, FKTN, DMD, COL6A1, SELENON, FKRP, SGCA, DYSF, CAPN3, SGCG, ANO5, DAG1, SGCD, TTN, SGCB, TRIM32, PRIMA1, TCAP, BCHE, ACHE, DES, LMNA, PLEC, LDB3, TRIM63, CAV3, CAVIN1, TOR1AIP1, POMGNT1, POMT1, COL6A3, COL6A2, GMPPB, POMT2, LARGE1, BAG3, CHKB, B3GALNT2, DNAJB6, CRPPA, NR0B1, B4GAT1, LIMS2, POMGNT2, INPP5K, RXYLT1, BVES, SYNE2, SYNE1, TNPO3, BEST1, PSAT1, NEB, SIL1, PMM2, RYR1, HSPB8, PIEZO2, PHGDH, HNRNPA2B1, DOK7, RIF1, DPM1, BUB3, DPM3, TRIP13, TRIP4, POMK, CEP57, TMEM43, PNKP, PYROXD1, TTN-AS1, HNRNPA1, BUB1B, COL4A1, CRYAB, AHCY, MSTN, GK, COL12A1, BUB1, EMD, UTRN, SSPN, IGF1, TRIM72, MYOT, SMCHD1, FSHMD1A, LTBP4, DMPK, ANO1, MB, TRPV2, LRRC7, ANPEP, CCN2, TRAF3, HMGCR, FRG1, FLNC, FHL1, HSPA8, MYOF, STAT5A, SPP1, CHKA, SGCE, DTNA, ANXA6, ORAI1, FST, IL6, DUX4, TNFRSF11B, ACTB, KITLG, MIR21, JAG1, ITGA7, NR3C2, LIF, CUX1, MMD, DCN, MIR222, LARGE2, MIR29C, NAT9, MIR188, MIR146A, MIR130B, KIF7, SUN1, DLG4, MIR30C1, DPEP1, DUSP6, CELF1, B3GNT2, GJB6, CCR2, WWP1, MIR486-1, ACE, DNMT3B, DUSP10, DNAH8, MIR340, MIR30C2, ACTN3, HPGDS, ACVR2B, LAMA1, MUL1, HAMP, TRAPPC11, AQP4, AQP1, APRT, EGFLAM, TNFAIP8L2, TOR1A, ANXA2, SETD7, OBSCN, ANXA1, B4GALNT2, TPH2, KIDINS220, BGN, CMD1B, CD38, EFEMP2, PCSK9, TRAT1, SIDT2, ZCCHC17, PARP1, ANO6, POGLUT1, ANO10, COL22A1, MSTO1, RUNX1T1, CBLL2, AGL, MCOLN1, MSC, PPIF, MMP10, MSN, MYOD1, HLA-C, NPC1, NPPA, P2RX7, SERPINE1, PRKN, PEG3, PIK3C2A, PITX2, PLAT, HIVEP1, HCFC1, PNN, PPARD, PPID, PRG2, PKN1, MPZ, MMP9, MATR3, MMP8, IDH2, IL1B, IL2RB, IMPA1, INPP5B, ITPR1, ITPR3, KRT14, LAMB2, LCN2, LGALS3, HLA-E, LMNB1, LPA, SMAD3, MAFD2, MBL2, MCL1, MFAP1, MAP2K6, RAG1, RAG2, PLAAT4, WNT7A, CNBP, PABPN1, GCY, TNFSF11, TNFRSF11A, BANF1, DPM2, SYNJ1, SYNJ2, MGAM, FMR1, HP, KL, ADIPOQ, ESR2, GOSR2, ENO1, HDAC9, GEM, VDAC3, GH1, GJB1, REN, BRD2, ROS1, GPT, S100B, SDC2, GLB1, GJB2, SHOX, TIMP1, SI, SMN1, SNTB1, SOD1, SPN, STIM1, TERF1, TGFB1, ABCA4
    • Congenital Muscular Dystrophy Orphanet
      Congenital muscular dystrophy (CMD) is a heterogeneous group of neuromuscular disorders with onset at birth or infancy characterized by hypotonia, muscle wasting, weakness or delayed motor milestones. The group includes myopathies with abnormalities at different cellular levels: the extracellular matrix (MDC1A, UCMD; see these terms), the dystrophin-associated glycoprotein complex (alphadystroglycanopathies, integrinopathies see these terms), the endoplasmic reticulum (rigid spine syndrome [RSMD1], and the nuclear envelope (LMNA-related CMD; [L-CMD] and Nesprin-1-related CMD; see these terms). Epidemiology The prevalence of CMDs is not well known but is estimated at about 1-9/100,000 in countries where they are most frequent. Males and females are equally affected. Clinical description Orthopaedic and respiratory complications that may be life-threatening often develop in the course of the disease. Etiology CMDs have autosomal recessive inheritance with the exception of dominant mutations possible in at least two forms (UCMD may have autosomal dominant or recessive inheritance; L-CMD is due to dominant de novo mutations).
    • Muscular Dystrophy Wikipedia
      Muscular dystrophy In affected muscle (right), the tissue has become disorganized and the concentration of dystrophin (green) is greatly reduced, compared to normal muscle (left). Specialty Pediatrics , medical genetics Symptoms Increasing weakening, breakdown of skeletal muscles , trouble walking [1] [2] Duration Long term [1] Types > 30 including Duchenne muscular dystrophy , Becker muscular dystrophy , facioscapulohumeral muscular dystrophy , limb-girdle muscular dystrophy , myotonic dystrophy [1] [2] Causes Genetic ( X-linked recessive , autosomal recessive , or autosomal dominant ) [2] Diagnostic method Blood tests , genetic testing [2] Treatment Physical therapy , braces , corrective surgery , assisted ventilation [1] [2] Prognosis Depends on the type [1] Muscular dystrophy ( MD ) is a group of muscle diseases that results in increasing weakening and breakdown of skeletal muscles over time. [1] The disorders differ in which muscles are primarily affected, the degree of weakness, how fast they worsen, and when symptoms begin. [1] Many people will eventually become unable to walk. [2] Some types are also associated with problems in other organs . [2] The muscular dystrophy group contains thirty different genetic disorders that are usually classified into nine main categories or types. [1] [2] The most common type is Duchenne muscular dystrophy (DMD), which typically affects males beginning around the age of four. [1] Other types include Becker muscular dystrophy , facioscapulohumeral muscular dystrophy , limb-girdle muscular dystrophy , and myotonic dystrophy . [1] They are due to mutations in genes that are involved in making muscle proteins. [2] This can occur due to either inheriting the defect from one's parents or the mutation occurring during early development . [2] Disorders may be X-linked recessive , autosomal recessive , or autosomal dominant . [2] Diagnosis often involves blood tests and genetic testing . [2] There is no cure for muscular dystrophy. [1] Physical therapy , braces , and corrective surgery may help with some symptoms. [1] Assisted ventilation may be required in those with weakness of breathing muscles . [2] Medications used include steroids to slow muscle degeneration, anticonvulsants to control seizures and some muscle activity, and immunosuppressants to delay damage to dying muscle cells . [1] Outcomes depend on the specific type of disorder. [1] Duchenne muscular dystrophy, which represents about half of all cases of muscular dystrophy, affects about one in 5,000 males at birth. [2] Muscular dystrophy was first described in the 1830s by Charles Bell . [2] The word "dystrophy" is from the Greek dys , meaning "difficult" and troph meaning "nourish". [2] Gene therapy , as a treatment, is in the early stages of study in humans. [2] Contents 1 Signs and symptoms 2 Cause 3 Diagnosis 3.1 Classification 4 Management 5 Prognosis 6 History 7 Research 8 See also 9 References 10 Further reading 11 External links Signs and symptoms [ edit ] The signs and symptoms consistent with muscular dystrophy are: [3] Progressive muscular wasting Poor balance Scoliosis (curvature of the spine and the back) Progressive inability to walk Waddling gait Calf deformation Limited range of movement Respiratory difficulty Cardiomyopathy Muscle spasms Gowers' sign Cause [ edit ] Dystrophin These conditions are generally inherited , and the different muscular dystrophies follow various inheritance patterns. Muscular dystrophy can be inherited by individuals as an X-linked disorder, a recessive or dominant disorder. Furthermore, it can be a spontaneous mutation which means errors in the replication of DNA and spontaneous lesions. Spontaneous lesions are due to natural damage to DNA, where the most common are depurination and deamination. [4] [5] Dystrophin protein is found in muscle fiber membrane; its helical nature allows it to act like a spring or shock absorber.
    • Muscular Dystrophy Gard
      Muscular dystrophy (MD) refers to a group of more than 30 genetic diseases characterized by progressive weakness and degeneration of the skeletal muscles that control movement. Some forms of MD are seen in newborns, infants or children, while others have late-onset and may not appear until middle age or later. The disorders differ in terms of the distribution and extent of muscle weakness (some forms of MD also affect cardiac muscle), age of onset, rate of progression, and pattern of inheritance. The prognosis for people with MD varies according to the type and progression of the disorder. There is no specific treatment to stop or reverse any form of MD. Treatment is supportive and may include physical therapy, respiratory therapy, speech therapy, orthopedic appliances used for support, corrective orthopedic surgery, and medications including corticosteroids, anticonvulsants (seizure medications), immunosuppressants, and antibiotics.
  • Ritscher-Schinzel Syndrome Gene_reviews
    Treatment of manifestations: Standard treatment for obesity, obstructive sleep apnea, cleft palate, congenital heart defects, hypercholesterolemia, renal anomalies, immunodeficiency, and developmental delay / intellectual disability. Surveillance : Measurement of growth parameters (particularly weight); assessment of developmental progress, mobility, self-help skills, and educational needs; and monitoring for symptoms of obstructive sleep apnea at each visit; ophthalmology evaluation annually or as clinically indicated; measurement of lipid profile periodically starting in childhood. ... In those w/obesity who have symptoms of sleep apnea Craniofacial Clinical assessment for cleft palate &/or micrognathia Consider referral to craniofacial clinic. ... Treatment of Manifestations in Individuals with Ritscher-Schinzel Syndrome View in own window Manifestation/Concern Treatment Considerations/Other Obesity Standard treatment Incl referral to nutritional specialists to monitor food intake & weight Obstructive sleep apnea Standard treatment May incl weight control, removal of tonsils/adenoids, &/or CPAP Cleft palate Standard surgical treatment, ideally by a specialized craniofacial team Congenital heart defects Standard treatment Hypercholesterolemia Standard treatment incl consideration of oral HMG-CoA reductase inhibitors (statins) 1 Other considerations incl optimizing weight, ↑ physical activity, & optimizing dietary fiber intake Renal anomalies Standard treatment per urologist &/or nephrologist Immunodeficiency Standard treatment per immunologist Family/Community Ensure appropriate social work involvement to connect families w/local resources, respite, & support. ... Recommended Surveillance for Individuals with Ritscher-Schinzel Syndrome View in own window System/Concern Evaluation Frequency Eyes Ophthalmology evaluation Annually or as clinically indicated Cardiovascular Lipid profile 1 Periodically 2 Constitutional Measurement of growth parameters, particularly weight Each visit Respiratory Monitor for symptoms of obstructive sleep apnea. Musculoskeletal Physical medicine, OT/PT assessment of mobility, self-help skills Development Monitor developmental progress & educational needs.
    WASHC5, CCDC22, DPH1, TBX1
    • Ritscher-Schinzel Syndrome 2 Omim
      A number sign (#) is used with this entry because of evidence that Ritscher-Schinzel syndrome-2 (RTSC2) is caused by mutation in the CCDC22 gene (300859) on chromosome Xp11. Description Ritscher-Schinzel syndrome-2 is an X-linked recessive syndromic form of intellectual disability associated with posterior fossa defects, cardiac malformations, and minor abnormalities of the face and distal extremities (summary by Kolanczyk et al., 2015). For a discussion of genetic heterogeneity of Ritscher-Schinzel syndrome, see RTSC1 (220210). Clinical Features Voineagu et al. (2012) reported a large family (IGOLD #586) in which 6 males spanning 3 generations had syndromic X-linked intellectual disability. One patient was deceased; clinical information was available for 5 patients, but the information given in a table was somewhat variable and unclear as to which individual had which features.
    • 3c Syndrome Orphanet
      Cranio-cerebello-cardiac (3C) syndrome is a rare multiple congenital anomalies syndrome characterized by craniofacial (prominent occiput and forehead, hypertelorism, ocular coloboma, cleft palate), cerebellar (Dandy-Walker malformation, cerebellar vermis hypoplasia) and cardiac (tetralogy of Fallot, atrial and ventricular septal defects) anomalies (see these terms). Epidemiology To date < 50 cases have been described. The syndrome appears to be panethnic. Clinical description 3C syndrome is a congenital disorder characterized by distinctive craniofacial features including, in decreasing frequency, low-set ears, hypertelorism, down-slanting palpebral fissures, depressed nasal bridge, prominent occiput, prominent forehead, cleft palate, micrognathia, ocular coloboma. Additional craniofacial features encompass nevus flammeus (on forehead), low posterior hairline, sparse scalp hair, eyebrows and eyelashes, open mouth with protruding tongue, and short neck. In 80% of cases, cerebellar anomalies are present and include primarily Dandy-Walker malformation or Dandy-Walker variant, cerebellar vermis hypoplasia and enlargement of cisterna magma.
    • 3c Syndrome Wikipedia
      3C syndrome Other names CCC dysplasia , Craniocerebellocardiac dysplasia [1] or Ritscher–Schinzel syndrome , [2] Specialty Medical genetics 3C syndrome is a rare condition whose symptoms include heart defects , cerebellar hypoplasia , and cranial dysmorphism . It was first described in the medical literature in 1987 by Ritscher and Schinzel, for whom the disorder is sometimes named. Contents 1 Signs and symptoms 2 Genetics 3 Diagnosis 3.1 Differential diagnosis 4 Management 5 Prognosis 6 Epidemiology 7 History 8 Other animals 9 References 10 External links Signs and symptoms [ edit ] The classical triad of symptoms that defines 3C syndrome includes certain heart defects, hypoplasia (underdevelopment) of the cerebellum , and cranial dysmorphisms, which can take various forms. The heart defects and cranial dysmorphisms are heterogeneous in individuals who are all classed as having Ritscher-Schinzel syndrome. [2] Heart defects commonly seen with Ritscher-Schinzel syndrome are associated with the endocardial cushion and are the most important factor in determining a diagnosis. The mitral valve and tricuspid valve of the heart can be malformed, the atrioventricular canal can be complete instead of developing into the interatrial septum and interventricular septum , and conotruncal heart defects , which include tetralogy of Fallot , double outlet right ventricle , transposition of the great vessels , [2] and hypoplastic left heart syndrome .
    • Ritscher-Schinzel Syndrome 1 Omim
      A number sign (#) is used with this entry because Ritscher-Schinzel syndrome-1 (RTSC1) is caused by homozygous mutation in the KIAA0196 gene (WSHC5; 610657) on chromosome 8q24. Description The 3C syndrome, also known as Ritscher-Schinzel syndrome, is a developmental malformation syndrome characterized by craniofacial abnormalities, congenital heart defects, and cerebellar brain malformations. Facial features include prominent occiput, prominent forehead, low-set ears, downslanting palpebral fissures, depressed nasal bridge, and micrognathia. Cardiac defects can include septal defects and aortic stenosis, among others, and brain imaging shows Dandy-Walker malformation, cerebellar vermis hypoplasia, posterior fossa cysts, and ventricular dilatation. Affected individuals have severe developmental delay (summary by Leonardi et al., 2001; Seidahmed et al., 2011).
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