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  • Late Talker Wikipedia
    Topics related to Speech-Language Pathology v t e Diseases of the nervous system , primarily CNS Inflammation Brain Encephalitis Viral encephalitis Herpesviral encephalitis Limbic encephalitis Encephalitis lethargica Cavernous sinus thrombosis Brain abscess Amoebic Brain and spinal cord Encephalomyelitis Acute disseminated Meningitis Meningoencephalitis Brain / encephalopathy Degenerative Extrapyramidal and movement disorders Basal ganglia disease Parkinsonism PD Postencephalitic NMS PKAN Tauopathy PSP Striatonigral degeneration Hemiballismus HD OA Dyskinesia Dystonia Status dystonicus Spasmodic torticollis Meige's Blepharospasm Athetosis Chorea Choreoathetosis Myoclonus Myoclonic epilepsy Akathisia Tremor Essential tremor Intention tremor Restless legs Stiff-person Dementia Tauopathy Alzheimer's Early-onset Primary progressive aphasia Frontotemporal dementia / Frontotemporal lobar degeneration Pick's Dementia with Lewy bodies Posterior cortical atrophy Vascular dementia Mitochondrial disease Leigh syndrome Demyelinating Autoimmune Inflammatory Multiple sclerosis For more detailed coverage, see Template:Demyelinating diseases of CNS Episodic/ paroxysmal Seizures and epilepsy Focal Generalised Status epilepticus For more detailed coverage, see Template:Epilepsy Headache Migraine Cluster Tension For more detailed coverage, see Template:Headache Cerebrovascular TIA Stroke For more detailed coverage, see Template:Cerebrovascular diseases Other Sleep disorders For more detailed coverage, see Template:Sleep CSF Intracranial hypertension Hydrocephalus Normal pressure hydrocephalus Choroid plexus papilloma Idiopathic intracranial hypertension Cerebral edema Intracranial hypotension Other Brain herniation Reye syndrome Hepatic encephalopathy Toxic encephalopathy Hashimoto's encephalopathy Both/either Degenerative SA Friedreich's ataxia Ataxia–telangiectasia MND UMN only: Primary lateral sclerosis Pseudobulbar palsy Hereditary spastic paraplegia LMN only: Distal hereditary motor neuronopathies Spinal muscular atrophies SMA SMAX1 SMAX2 DSMA1 Congenital DSMA Spinal muscular atrophy with lower extremity predominance (SMALED) SMALED1 SMALED2A SMALED2B SMA-PCH SMA-PME Progressive muscular atrophy Progressive bulbar palsy Fazio–Londe Infantile progressive bulbar palsy both: Amyotrophic lateral sclerosis v t e Dyslexia and related specific developmental disorders Conditions Speech, language , and communication Expressive language disorder Infantile speech Landau–Kleffner syndrome Language disorder Lisp Mixed receptive-expressive language disorder Specific language impairment Speech and language impairment Speech disorder Speech error Speech sound disorder Stuttering Tip of the tongue Learning disability Dyslexia Dyscalculia Dysgraphia Disorder of written expression Motor Developmental coordination disorder Developmental verbal dyspraxia Sensory Auditory processing disorder Sensory processing disorder Related topics Dyslexia research Irlen filters Learning Ally Learning problems in childhood cancer Literacy Management of dyslexia Multisensory integration Neuropsychology Reading acquisition Spelling Writing system Lists Dyslexia in fiction Languages by Writing System People with dyslexia v t e Mental and behavioral disorders Adult personality and behavior Gender dysphoria Ego-dystonic sexual orientation Paraphilia Fetishism Voyeurism Sexual maturation disorder Sexual relationship disorder Other Factitious disorder Munchausen syndrome Intermittent explosive disorder Dermatillomania Kleptomania Pyromania Trichotillomania Personality disorder Childhood and learning Emotional and behavioral ADHD Conduct disorder ODD Emotional and behavioral disorders Separation anxiety disorder Movement disorders Stereotypic Social functioning DAD RAD Selective mutism Speech Stuttering Cluttering Tic disorder Tourette syndrome Intellectual disability X-linked intellectual disability Lujan–Fryns syndrome Psychological development ( developmental disabilities ) Pervasive Specific Mood (affective) Bipolar Bipolar I Bipolar II Bipolar NOS Cyclothymia Depression Atypical depression Dysthymia Major depressive disorder Melancholic depression Seasonal affective disorder Mania Neurological and symptomatic Autism spectrum Autism Asperger syndrome High-functioning autism PDD-NOS Savant syndrome Dementia AIDS dementia complex Alzheimer's disease Creutzfeldt–Jakob disease Frontotemporal dementia Huntington's disease Mild cognitive impairment Parkinson's disease Pick's disease Sundowning Vascular dementia Wandering Other Delirium Organic brain syndrome Post-concussion syndrome Neurotic , stress -related and somatoform Adjustment Adjustment disorder with depressed mood Anxiety Phobia Agoraphobia Social anxiety Social phobia Anthropophobia Specific social phobia Specific phobia Claustrophobia Other Generalized anxiety disorder OCD Panic attack Panic disorder Stress Acute stress reaction PTSD Dissociative Depersonalization disorder Dissociative identity disorder Fugue state Psychogenic amnesia Somatic symptom Body dysmorphic disorder Conversion disorder Ganser syndrome Globus pharyngis Psychogenic non-epileptic seizures False pregnancy Hypochondriasis Mass psychogenic illness Nosophobia Psychogenic pain Somatization disorder Physiological and physical behavior Eating Anorexia nervosa Bulimia nervosa Rumination syndrome Other specified feeding or eating disorder Nonorganic sleep Hypersomnia Insomnia Parasomnia Night terror Nightmare REM sleep behavior disorder Postnatal Postpartum depression Postpartum psychosis Sexual dysfunction Arousal Erectile dysfunction Female sexual arousal disorder Desire Hypersexuality Hypoactive sexual desire disorder Orgasm Anorgasmia Delayed ejaculation Premature ejaculation Sexual anhedonia Pain Nonorganic dyspareunia Nonorganic vaginismus Psychoactive substances, substance abuse and substance-related Drug overdose Intoxication Physical dependence Rebound effect Stimulant psychosis Substance dependence Withdrawal Schizophrenia , schizotypal and delusional Delusional Delusional disorder Folie à deux Psychosis and schizophrenia-like Brief reactive psychosis Schizoaffective disorder Schizophreniform disorder Schizophrenia Childhood schizophrenia Disorganized (hebephrenic) schizophrenia Paranoid schizophrenia Pseudoneurotic schizophrenia Simple-type schizophrenia Other Catatonia Symptoms and uncategorized Impulse control disorder Klüver–Bucy syndrome Psychomotor agitation Stereotypy v t e Allied health professions Anesthesia technician Aquatic therapist Athletic trainer Audiologist Dental hygienist Dietitian Cardiac physiologist Emergency medical services Hemodialysis technicians Massage therapist Medical assistants Medical coder Medical physicist Medical technologist Medical transcription Music and arts therapist Nutrition ( clinical ) Occupational therapist Optometrist Phlebotomist Orthotist / Prosthetist Physical therapist Clinical psychologist Public health Radiation therapist Radiographer Respiratory therapy Social worker Speech therapist Orthoptists v t e Pervasive developmental disorders and autism spectrum Main Causes Comorbid conditions Epidemiology Heritability Societal and cultural aspects Medical model Therapies Diagnoses Autism spectrum ( High-functioning autism Classic autism Asperger syndrome Pervasive developmental disorder not otherwise specified Childhood disintegrative disorder Rett syndrome ) Related conditions Alexithymia Attention deficit hyperactivity disorder Anxiety disorder ( obsessive–compulsive disorder ) Late talker Epilepsy Fragile X syndrome Hyperlexia Savant syndrome Sensory processing disorder Intellectual disability Developmental coordination disorder Multiple complex developmental disorder Controversies Autism rights movement Autistic enterocolitis Facilitated communication MMR vaccine Rapid prompting method Thiomersal ( Chelation ) Diagnostic scales Gilliam Asperger's disorder scale Autism Diagnostic Observation Schedule Autism Diagnostic Interview Autism-spectrum quotient Childhood Autism Rating Scale Lists Autism-related topics Fictional characters Schools This developmental psychology –related article is a stub .
  • Navel Fetishism Wikipedia
    In Solomon 's lavish praise of his love – the country girl, Sulaimi – the navel is mentioned as follows: " thy navel is like a round goblet , which wanteth not liquor: thy belly is like a heap of wheat set about with lilies . " (7:2). [56] [57] [58] American poet May Swenson in her poem "Little Lion Face" wrote, " Now I'm bold to touch your swollen neck, put careful lips to slick petals, snuff up gold pollen in your navel cup. " [59] and poem "August Night" wrote, " Your navel a little pool in pulsing tide an aura round your knees ". [60] Czech -born writer Milan Kundera in his 2015 book The Festival of Insignificance conveys about the eroticism of exposed female navels. [61] [62] [63] Alain, one of the characters in the book, observes to his friend how most of the young women in Paris wear T-shirts or blouses that expose their midriffs, displaying their navels for all to see.
  • Battered Woman Syndrome Wikipedia
    He allegedly had attempted to break her ankles and burn her with a hot iron on the night of her attack. Accusing him of domestic violence and marital rape , she claimed provocation.
  • Female Genital Mutilation Wikipedia
    For example, in the northeastern regions of Ethiopia and Kenya, which share a border with Somalia, the Somali people practise FGM at around the same rate as they do in Somalia. [100] But in Guinea all Fulani women responding to a survey in 2012 said they had experienced FGM, [101] against 12 percent of the Fulani in Chad, while in Nigeria the Fulani are the only large ethnic group in the country not to practise it. [102] Reasons Support from women 1996 Pulitzer Prize for Feature Photography Kenyan FGM ceremony — Stephanie Welsh, Newhouse News Service [103] Dahabo Musa, a Somali woman, described infibulation in a 1988 poem as the "three feminine sorrows": the procedure itself, the wedding night when the woman is cut open, then childbirth when she is cut again. [104] Despite the evident suffering, it is women who organize all forms of FGM. [105] [r] Anthropologist Rose Oldfield Hayes wrote in 1975 that educated Sudanese men who did not want their daughters to be infibulated (preferring clitoridectomy) would find the girls had been sewn up after the grandmothers arranged a visit to relatives. [110] Gerry Mackie has compared the practice to footbinding .
  • Chytridiomycosis Wikipedia
    The rise in temperature has increased evaporation in certain forest environments that as a result has promoted cloud formation. [14] Experts propose that increased cloud cover might actually be decreasing the daytime temperature by blocking the sun, while at night the cloud cover serves as insulation to raise the nighttime temperature from its normal range.
  • Acne Wikipedia
    Generally speaking, retinoids increase the skin's sensitivity to sunlight and are therefore recommended for use at night. [1] Tretinoin is the least expensive of the topical retinoids and is the most irritating to the skin, whereas adapalene is the least irritating but costs significantly more. [1] [87] Most formulations of tretinoin are incompatible for use with benzoyl peroxide. [15] Tazarotene is the most effective and expensive topical retinoid but is not as well tolerated. [1] [87] Retinol is a form of vitamin A that has similar but milder effects and is present in many over-the-counter moisturizers and other topical products.
    • Acne, Adult OMIM
      Acne is principally a disorder of adolescence but persists into middle age in a small minority of individuals. Goulden et al. (1999) quoted evidence, primarily from twin studies, suggesting that acne may be an inherited disorder. Clinically, the condition consists of a spectrum of diseases varying in age of onset and resolution as well as in severity, type, and distribution of lesions. It can be argued that, when investigating the inheritance of acne, particular subgroups must be considered separately. Goulden et al. (1999) investigated the familial risk of persistent adult acne by studying the occurrence of this condition in first-degree relatives of patients with adult persistent acne compared with the relatives of unaffected volunteers.
  • Ear Pain Wikipedia
    Fever Hearing loss Pain may disrupt sleep Perforated tympanic membrane Discharge followed by pain improvement Mastoiditis * Children History of URI >10 days Recent history of URI or ear infection Fevers/chills May see signs of otitis media on exam Pain is located behind the ear with postauricular (i.e. near mastoid process ) swelling* Diagnose with CT Chronic suppurative otitis media Conductive hearing loss Relapsing/remitting or chronic discharge May see perforation of tympanic membrane or cholesteatoma on exam Serous otitis media (otitis media with effusion) No signs of infection Prominent hearing loss May have history of URI or acute otitis media Otitis externa Swimming Psoriasis Seborrheic dermatitis Q-tips in the ear Bilateral pain Scaling Itching Pain exacerbated when ear is pulled May see granulation tissue in canal on exam Necrotizing/malignant otitis externa* Diabetes Immuno-compromised Constant pain with increasing severity at night* Purulent discharge* Pain out of proportion to exam findings* Biopsy granulation tissue for culture Chondritis vs perichondritis Recent ear trauma (i.e. ear piercing) External ear appears inflamed Chondritis more likely than perichondritis if ear shape is distorted Referred causes Diagnosis Features [4] [8] [9] GERD Bilateral pain Neuralgia Pain described as tingling/sharp/burning sensation; episodes can start with light touch Malignancy* Weight loss* Arthritis of the neck Pain exacerbated by neck movement Eagle syndrome Swallowing exacerbates pain Infected 3 rd molar Extreme food temperatures exacerbate pain Temporal arteritis* Patient age > 50* Chewing exacerbates pain* TMJ dysfunction Patient grinds teeth Bilateral pain Pain + crepitus with TMJ palpation Jaw clicking *Indicates a "Can't Miss" diagnosis or a red flag.
    NF2, PDGFB, SMARCB1, SUFU, NHS, BATF2
  • Agoraphobia Wikipedia
    External links [ edit ] Classification D ICD - 10 : F40.0 ICD - 9-CM : 300.22 Without panic disorder, 300.21 With panic disorder MeSH : D000379 External resources MedlinePlus : 000923 Patient UK : Agoraphobia Agoraphobia at Curlie v t e Mental and behavioral disorders Adult personality and behavior Gender dysphoria Ego-dystonic sexual orientation Paraphilia Fetishism Voyeurism Sexual maturation disorder Sexual relationship disorder Other Factitious disorder Munchausen syndrome Intermittent explosive disorder Dermatillomania Kleptomania Pyromania Trichotillomania Personality disorder Childhood and learning Emotional and behavioral ADHD Conduct disorder ODD Emotional and behavioral disorders Separation anxiety disorder Movement disorders Stereotypic Social functioning DAD RAD Selective mutism Speech Stuttering Cluttering Tic disorder Tourette syndrome Intellectual disability X-linked intellectual disability Lujan–Fryns syndrome Psychological development ( developmental disabilities ) Pervasive Specific Mood (affective) Bipolar Bipolar I Bipolar II Bipolar NOS Cyclothymia Depression Atypical depression Dysthymia Major depressive disorder Melancholic depression Seasonal affective disorder Mania Neurological and symptomatic Autism spectrum Autism Asperger syndrome High-functioning autism PDD-NOS Savant syndrome Dementia AIDS dementia complex Alzheimer's disease Creutzfeldt–Jakob disease Frontotemporal dementia Huntington's disease Mild cognitive impairment Parkinson's disease Pick's disease Sundowning Vascular dementia Wandering Other Delirium Organic brain syndrome Post-concussion syndrome Neurotic , stress -related and somatoform Adjustment Adjustment disorder with depressed mood Anxiety Phobia Agoraphobia Social anxiety Social phobia Anthropophobia Specific social phobia Specific phobia Claustrophobia Other Generalized anxiety disorder OCD Panic attack Panic disorder Stress Acute stress reaction PTSD Dissociative Depersonalization disorder Dissociative identity disorder Fugue state Psychogenic amnesia Somatic symptom Body dysmorphic disorder Conversion disorder Ganser syndrome Globus pharyngis Psychogenic non-epileptic seizures False pregnancy Hypochondriasis Mass psychogenic illness Nosophobia Psychogenic pain Somatization disorder Physiological and physical behavior Eating Anorexia nervosa Bulimia nervosa Rumination syndrome Other specified feeding or eating disorder Nonorganic sleep Hypersomnia Insomnia Parasomnia Night terror Nightmare REM sleep behavior disorder Postnatal Postpartum depression Postpartum psychosis Sexual dysfunction Arousal Erectile dysfunction Female sexual arousal disorder Desire Hypersexuality Hypoactive sexual desire disorder Orgasm Anorgasmia Delayed ejaculation Premature ejaculation Sexual anhedonia Pain Nonorganic dyspareunia Nonorganic vaginismus Psychoactive substances, substance abuse and substance-related Drug overdose Intoxication Physical dependence Rebound effect Stimulant psychosis Substance dependence Withdrawal Schizophrenia , schizotypal and delusional Delusional Delusional disorder Folie à deux Psychosis and schizophrenia-like Brief reactive psychosis Schizoaffective disorder Schizophreniform disorder Schizophrenia Childhood schizophrenia Disorganized (hebephrenic) schizophrenia Paranoid schizophrenia Pseudoneurotic schizophrenia Simple-type schizophrenia Other Catatonia Symptoms and uncategorized Impulse control disorder Klüver–Bucy syndrome Psychomotor agitation Stereotypy
    CREBBP, SGCE, EP300, ADORA2A, GLRB, SCLY, TAL1, KRT7, HTR1A, GAD1, GRP, MIR22, NPSR1, TPH2, BDNF, CAMKK2, CRH, CRP, SLC6A4, SLC6A2, P2RX7, NPY, MAOA, ACE, OPN1SW, HCRTR1, HCRT, GRPR, MIR491
    • Agoraphobia Mayo Clinic
      Overview Agoraphobia (ag-uh-ruh-FOE-be-uh) is a type of anxiety disorder. Agoraphobia involves fearing and avoiding places or situations that might cause panic and feelings of being trapped, helpless or embarrassed. You may fear an actual or upcoming situation. For example, you may fear using public transportation, being in open or enclosed spaces, standing in line, or being in a crowd. The anxiety is caused by fear that there's no easy way to escape or get help if the anxiety gets overwhelming. You may avoid situations because of fears such as getting lost, falling, or having diarrhea and not being able to get to a bathroom.
  • Hellp Syndrome Wikipedia
    These symptoms may also become more severe at night. [8] [9] [10] [11] [12] As the condition progresses and worsens, a spontaneous hematoma occurs following the rupture of the liver capsule, which occurs more frequently in the right lobe.
    CD46, CFH, CFI, HELLPAR, FASLG, FAS, PGF, F5, LEP, HADHA, F2, TNF, HPGDS, LGALS13, FLT1, VEGFA, MTHFR, MAPK14, TLR4, AIMP2, TLR2, MAPK3, TPBG, VEGFC, TGFB3, VWF, MAPK1, ABCG2, TFPI2, IL18R1, GRAP2, EBI3, AHSA1, ADAMTS13, SIRT4, RNF19A, POLDIP2, SLC17A5, ERVW-1, MBL3P, AHSP, NOD2, POTEF, SERPINE2, ACTB, SERPINE1, PAH, APC, CFB, CA9, CD40LG, CD59, CDKN1C, COX8A, CP, CRK, ENG, EPHX1, GAPDH, GNB3, GPT, NR3C1, GSTM1, GSTT1, HSPA4, HSPG2, IFNG, IL1B, IL1RN, CXCL8, IL10, LEPR, LNPEP, ADM, NOS3, PAEP, MBL2
    • Hellp Syndrome Orphanet
      A rare hemorrhagic disorder due to an acquired platelet anomaly characterized by hemolysis, elevated liver enzymes and thrombocytopenia that affects pregnant or post-partum women, and is frequently associated with severe preeclampsia. Symptoms are variable, typically including right upper quadrant or epigastric abdominal pain, nausea, vomiting, excessive weight gain, generalized edema, hypertension, general malaise, right shoulder pain, backache, and/or headache. Hepatic hemorrhage and rupture, renal failure, and pulmonary edema can result in maternal and/or fetal death.
    • Hellp Syndrome GARD
      HELLP syndrome is a life-threatening condition that can potentially complicate pregnancy. It is named for 3 features of the condition: H emolysis, E levated L iver enzyme levels, and L ow P latelet levels. It typically occurs in the last 3 months of pregnancy (the third trimester) but can also start soon after delivery. A wide range of non-specific symptoms may be present in women with HELLP syndrome. Symptoms may include fatigue; malaise; fluid retention and excess weight gain; headache; nausea and vomiting; pain in the upper right or middle of the abdomen; blurry vision; and rarely, nosebleed or seizures.
  • Intravascular Lymphomas Wikipedia
    They commonly present with skin lesions, less commonly symptoms due to central nervous system involvement, and in a minority of cases symptoms due to the involvement of the bone marrow, liver, kidneys, ovaries, and/or cervix . [1] They often show signs of an disseminated disease such as fever, weight loss, night sweats , arthralgias , jaundice , decreased numbers of circulating red blood cells , white blood cells , and/or platelets , bone marrow involvement as determined by biopsy , and signs/symptoms of multiple organ involvement. [8] Diagnosis [ edit ] The diagnosis of IVNK/TL depends upon obtaining histology findings in the skin and/or other involved tissue that resembles that seen in IVBCL except that the malignant lymphocytes are not B-cells but rather: 1) NK-cells as evidenced by their expression of NK-cell selective marker proteins (e.g.
    BCL6, BCL2, TNFRSF8, CD274, SMUG1, ACP3, LAMC2, KRT20, PRTN3, MME, KMT2A, IGH, IRF4, ALK, CSF3, CSF2, CRP, MS4A1, PWWP3A
    • Intravascular Large B-Cell Lymphoma Orphanet
      Intravascular large B-cell lymphoma (IVLBCL) is a very rare form of diffuse large B-cell lymphoma (see this term) characterized by the selective growth of lymphoma cells within the lumina of small blood vessels (especially the capillaries) that most often presents with a wide range of clinical manifestations (as potentially any tissue can be involved), with patients from Western countries more frequently manifesting with neurological and cutaneous symptoms while patients from Asian countries more frequently displaying hepatosplenomegaly and thrombocytopenia. IVLBCL is characterized by an absence of lymphadenopathy, an aggressive clinical course and a poor prognosis.
  • Emergent Virus Wikipedia
    . ^ National Science Foundation. "The Night Life: Why We Need Bats All the Time-Not Just on Halloween" .
  • Sinusitis Wikipedia
    People with migraines do not typically have the thick nasal discharge that is a common symptom of a sinus infection. [14] Chronic [ edit ] Symptoms may include any combination of: nasal congestion , facial pain, headache , night-time coughing, an increase in previously minor or controlled asthma symptoms, general malaise , thick green or yellow discharge , feeling of facial fullness or tightness that may worsen when bending over, dizziness, aching teeth, and/or bad breath . [15] Often, chronic sinusitis can lead to anosmia , the inability to smell objects. [15] By location [ edit ] The four paired paranasal sinuses are the frontal, ethmoidal, maxillary, and sphenoidal sinuses. ... National Library of Medicine. 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 Common cold Viruses Adenovirus Coronavirus Enterovirus Rhinovirus Symptoms Cough Fatigue Fever Headache Loss of appetite Malaise Muscle aches Nasal congestion Rhinorrhea Sneezing Sore throat Weakness Complications Acute bronchitis Bronchiolitis Croup Otitis media Pharyngitis Pneumonia Sinusitis Strep throat Drugs Antiviral drugs Pleconaril (experimental) Authority control NDL : 00576408
    CFTR, IL13, RSPH4A, AZGP1, MET, PIP, PPP1R9B, PRTN3, PNP, PTPN22, CXCR4, MGP, CIITA, NBN, NCF2, NCF4, PIK3R1, CYBC1, TCF3, WIPF1, PSMB4, PSMB9, WAS, LRRC8A, CCDC40, RFX5, RFXAP, DNAI1, NME8, DNAAF1, BLNK, CYBB, BLM, RUNX2, RFXANK, CD79A, CD79B, NCF1, DNAAF3, CTLA4, CYBA, IL2RG, DNMT3B, FMR1, HLA-DPA1, HLA-DPB1, ATM, IRF8, CFI, IGHM, IGLL1, IKBKB, ADA, BTK, CCL5, IL6, HIF1A, MUC5AC, IL5, DICER1, IL33, IL22, ASCC1, SMOX, GORASP1, WNK1, PDPN, AP5B1, CLEC4D, MUC5B, POSTN, AAVS1, SLC9A6, ACR, CD40, CLU, CSF2, IL1A, IL1B, CXCL8, IL17A, LTC4S, NFKB1, SERPINE1, PTGDS, ARHGEF7, RAG2, RELA, CCL7, CCL11, SLC5A5, SYT1, TNF, VEGFA, ST8SIA4, EPX, H3P40
  • Anti-Catholicism Wikipedia
    Catholic membership in Britain continues to grow, thanks to the immigration of Irish and more recently Polish workers. [23] Conflict and rivalry between Catholicism and Protestantism since the 1920s, and especially since the 1960s, has centred on the Troubles in Northern Ireland . [24] Anti-Catholicism in Britain was long represented by the burning of an effigy of the Catholic conspirator Guy Fawkes at widespread celebrations on Guy Fawkes Night every 5 November. [25] However, this celebration has lost most of its anti-Catholic connotations. ... Clergy, nuns and lay leaders began to be targeted, leading to thousands of arrests over the ensuing years, often on trumped up charges of currency smuggling or "immorality". [87] In Hitler's Night of the Long Knives purge, Erich Klausener , the head of Catholic Action , was assassinated. [88] Adalbert Probst , national director of the Catholic Youth Sports Association, Fritz Gerlich , editor of Munich's Catholic weekly and Edgar Jung , one of the authors of the Marburg speech , were among the other Catholic opposition figures killed in the purge. [89] By 1937, the Church hierarchy in Germany, which had initially attempted to co-operate with the new government, had become highly disillusioned.
  • Diabetes In Dogs Wikipedia
    The main symptoms which occur in nearly all dogs with diabetes mellitus are: [48] excessive water consumption, excessive water consumption due to too much thirstiness, this condition is often called polydipsia. [48] frequent and/or excessive urination, known as polyuria , often requiring the dog to be let outside to urinate during the night, [49] greater than average appetite, increased appetite to abnormal levels, which is too greater than the average appetite, a condition known as polyphagai. , [47] [48] weight loss, dogs with diabetes may also suffer from severe weight loss, weakness , anorexia and blindness. [48] Sometimes, the first sign of diabetes noticed by the owner may be that their dog either has become blind (due to the formation of cataracts in the eyes), or has vomiting, anorexia, lethargy and weakness (due to ketoacidosis). [49] Diabetes mellitus can be a threat to the health of the dog since it may cause urinary tract infections.
  • Waldenström's Macroglobulinemia Wikipedia
    They recommended starting therapy in patients with constitutional symptoms such as recurrent fever , night sweats , fatigue due to anemia , weight loss , progressive symptomatic lymphadenopathy or spleen enlargement , and anemia due to bone marrow infiltration.
    MYD88, PAX5, IGH, LPL, CXCR4, ANPEP, MYC, ZAP70, MALT1, CDR3, MYOM2, SDC1, CXCL12, AIMP2, TCL1A, GRAP2, TCL1B, AHSA1, ACSBG1, RNF19A, IBTK, POLDIP2, IGHV4-34, BCL11A, KRT20, EXOC2, RAPH1, MAPK1, NOS1, NOTCH2, NOS2, BCL6, BCL9, BLM, BRAF, BSG, BTK, SERPING1, CCND3, CD6, MS4A1, TNFRSF8, CD40LG, CD79A, CRK, MAPK14, CTNNB1, IL4, IRF4, CD200, NCAM1, CCND1, SLC35B2
  • Extranodal Nk/t-Cell Lymphoma, Nasal Type Wikipedia
    In these cases, there is relatively little involvement of lymph nodes except as a result of direct invasion from non-nodal sites. [12] Thirty-five to forty-five percent of patients present with a history of malaise , fever , night sweats , and/or weight loss . Most (70-75%) patients are diagnosed with early stage I or II disease while the rest have far more serious stage III or IV disease.
    JAK3, STAT5B, CFLAR, ASRGL1, NCAM1, PDLIM7, TNFRSF8, PRDM1, SOAT1, TRBV20OR9-2, ASPG, TMTC3, CREBZF, CD274, STAT3, ABO, GNLY, TP53, KRT20, PDCD1, ABCB1, MS4A1, EZH2, MYC, MME, BCL2, HAVCR2, ELF4, ETS1, BCOR, FCGR3A, TBC1D9, PLK2, FCGR3B, GZMH, GZMB, EOMES, IL2, TNFAIP3, TIA1, IL4, KIT, KLRD1, LAG3, SLC22A2, PTPRC, POU2F2, PLOD2, ADM, MEFV, NOS2, NOS1, MIR223
  • Angular Cheilitis Wikipedia
    Secondly, there may be a need to increase the vertical dimension of the lower face to prevent overclosure of the mouth and formation of deep skin folds. [24] This may require the construction of a new denture with an adjusted bite. [4] Rarely, in cases resistant to normal treatments, surgical procedures such as collagen injections (or other facial fillers such as autologous fat or crosslinked hyaluronic acid ) are used in an attempt to restore the normal facial contour. [2] [4] Other measures which seek to reverse the local factors that may be contributing to the condition include improving oral hygiene , stopping smoking or other tobacco habits and use of a barrier cream (e.g. zinc oxide paste) at night. [2] Thirdly, treatment of the infection and inflammation of the lesions themselves is addressed. ... External links [ edit ] Classification D ICD - 10 : K13.0 ICD - 9-CM : 528.5 , 686.8 MeSH : D002613 Wikimedia Commons has media related to Angular cheilitis . v t e Oral and maxillofacial pathology Lips Cheilitis Actinic Angular Plasma cell Cleft lip Congenital lip pit Eclabium Herpes labialis Macrocheilia Microcheilia Nasolabial cyst Sun poisoning Trumpeter's wart Tongue Ankyloglossia Black hairy tongue Caviar tongue Crenated tongue Cunnilingus tongue Fissured tongue Foliate papillitis Glossitis Geographic tongue Median rhomboid glossitis Transient lingual papillitis Glossoptosis Hypoglossia Lingual thyroid Macroglossia Microglossia Rhabdomyoma Palate Bednar's aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus Oral mucosa – Lining of mouth Amalgam tattoo Angina bullosa haemorrhagica Behçet's disease Bohn's nodules Burning mouth syndrome Candidiasis Condyloma acuminatum Darier's disease Epulis fissuratum Erythema multiforme Erythroplakia Fibroma Giant-cell Focal epithelial hyperplasia Fordyce spots Hairy leukoplakia Hand, foot and mouth disease Hereditary benign intraepithelial dyskeratosis Herpangina Herpes zoster Intraoral dental sinus Leukoedema Leukoplakia Lichen planus Linea alba Lupus erythematosus Melanocytic nevus Melanocytic oral lesion Molluscum contagiosum Morsicatio buccarum Oral cancer Benign: Squamous cell papilloma Keratoacanthoma Malignant: Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker's melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga–Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus Teeth ( pulp , dentin , enamel ) Amelogenesis imperfecta Ankylosis Anodontia Caries Early childhood caries Concrescence Failure of eruption of teeth Dens evaginatus Talon cusp Dentin dysplasia Dentin hypersensitivity Dentinogenesis imperfecta Dilaceration Discoloration Ectopic enamel Enamel hypocalcification Enamel hypoplasia Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth Microdontia Odontogenic tumors Keratocystic odontogenic tumour Odontoma Dens in dente Open contact Premature eruption Neonatal teeth Pulp calcification Pulp stone Pulp canal obliteration Pulp necrosis Pulp polyp Pulpitis Regional odontodysplasia Resorption Shovel-shaped incisors Supernumerary root Taurodontism Trauma Avulsion Cracked tooth syndrome Vertical root fracture Occlusal Tooth loss Edentulism Tooth wear Abrasion Abfraction Acid erosion Attrition Periodontium ( gingiva , periodontal ligament , cementum , alveolus ) – Gums and tooth-supporting structures Cementicle Cementoblastoma Gigantiform Cementoma Eruption cyst Epulis Pyogenic granuloma Congenital epulis Gingival enlargement Gingival cyst of the adult Gingival cyst of the newborn Gingivitis Desquamative Granulomatous Plasma cell Hereditary gingival fibromatosis Hypercementosis Hypocementosis Linear gingival erythema Necrotizing periodontal diseases Acute necrotizing ulcerative gingivitis Pericoronitis Peri-implantitis Periodontal abscess Periodontal trauma Periodontitis Aggressive As a manifestation of systemic disease Chronic Perio-endo lesion Teething Periapical, mandibular and maxillary hard tissues – Bones of jaws Agnathia Alveolar osteitis Buccal exostosis Cherubism Idiopathic osteosclerosis Mandibular fracture Microgenia Micrognathia Intraosseous cysts Odontogenic : periapical Dentigerous Buccal bifurcation Lateral periodontal Globulomaxillary Calcifying odontogenic Glandular odontogenic Non-odontogenic: Nasopalatine duct Median mandibular Median palatal Traumatic bone Osteoma Osteomyelitis Osteonecrosis Bisphosphonate-associated Neuralgia-inducing cavitational osteonecrosis Osteoradionecrosis Osteoporotic bone marrow defect Paget's disease of bone Periapical abscess Phoenix abscess Periapical periodontitis Stafne defect Torus mandibularis Temporomandibular joints , muscles of mastication and malocclusions – Jaw joints, chewing muscles and bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing sialometaplasia Mucocele Ranula Pneumoparotitis Salivary duct stricture Salivary gland aplasia Salivary gland atresia Salivary gland diverticulum Salivary gland fistula Salivary gland hyperplasia Salivary gland hypoplasia Salivary gland neoplasms Benign: Basal cell adenoma Canalicular adenoma Ductal papilloma Monomorphic adenoma Myoepithelioma Oncocytoma Papillary cystadenoma lymphomatosum Pleomorphic adenoma Sebaceous adenoma Malignant: Acinic cell carcinoma Adenocarcinoma Adenoid cystic carcinoma Carcinoma ex pleomorphic adenoma Lymphoma Mucoepidermoid carcinoma Sclerosing polycystic adenosis Sialadenitis Parotitis Chronic sclerosing sialadenitis Sialectasis Sialocele Sialodochitis Sialosis Sialolithiasis Sjögren's syndrome Orofacial soft tissues – Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig's angina Macrostomia Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease
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  • Bloom Syndrome GeneReviews
    Recommended Surveillance for Individuals with Bloom Syndrome (BSyn) View in own window Manifestation Evaluation Frequency Wilms tumor Abdominal ultrasound Screen for signs/symptoms incl hematuria & a painless abdominal mass Every 3 mos from time of diagnosis to age 8 yrs Leukemia Screening & family education on signs/symptoms incl pallor, abnormal bleeding, petechiae, fatigue, unintentional weight loss Every health visit Lymphoma Screening & family education on signs/symptoms incl enlarged lymph nodes, unexplained fevers, drenching night sweats, fatigue, unintentional weight loss Every health visit Whole-body MRI Every 1-2 yrs from age 12-13 yrs Colorectal cancer Colonoscopy Annually from age 10-12 yrs Fecal immunochemical testing Every 6 mos from age 10-12 yrs Breast cancer Breast MRI in females Annually from age 18 yrs Skin cancer Skin examination w/dermatologist for any suspicious skin lesions On recognition of suspicious lesions & annually thereafter Diabetes mellitus Fasting blood glucose & hemoglobin A1C Screening & family education on signs/symptoms of polyuria, polydipsia, weight loss Annually from age 10 yrs Hypothyroidism Serum TSH w/reflex to T4 Screening & family education on signs/symptoms incl fatigue, constipation, cold sensitivity, weight gain Annually from age 10 yrs Dyslipidemia Lipid profile Annually from age 10 yrs Agents/Circumstances to Avoid Sun exposure to the face and other exposed areas, particularly in infancy and early childhood, should be avoided.
    BLM, UNG, NSMCE2, WRN, LIG1, TP53, ATM, RECQL4, HFM1, TOPBP1, GABPA, MYC, NFE2L2, FES, IL6, FANCC, GYPA, FANCM, TGFB1, RAD51, TNF, LBR, BRCA1, H2AX, EXO1, BRCA2, MPO, DNA2, MUS81, XRS, LTBP4, TP53BP1, CCL27, SOD1, SOD2, NXF1, MVP, TXN, NREP, UBE2I, TOP3A, HSPB3, ARID5A, TOP2B, ADAM15, TRBV20OR9-2, XPA, THY1, USO1, RAD54L, ACTB, SEC14L2, DMC1, TCHP, POLD4, HPSE2, TNMD, MCPH1, ASRGL1, BRIP1, SLX4, CHEK2, LCS1, TSLP, RMI2, FOXR2, NCF1, VPS9D1-AS1, IFT80, SLC12A9, ANKH, NAT10, RIF1, MS4A12, CYCS, NOX4, APOBEC3C, PDLIM3, SMR3A, FGF21, ATRNL1, SUMO3, SPIDR, SIRT1, TREX1, SUMO2, RAD51D, SMN2, FN1, FANCD2, FANCB, FANCF, FEN1, FGF2, FLNB, FXN, SMN1, MTOR, GP1BA, GPR17, GYPB, GYPE, HIF1A, ESR1, EIF4E, EIF2S1, EDNRA, DDX1, CYLD, CYBB, CRYGD, CDKN1A, CDA, SERPINH1, CBL, CAT, CASP3, ATR, ATHS, APRT, HLA-A, HSPB1, HSPB2, PITX3, SLPI, SELP, CCL2, SCN5A, SCD, SERPINB3, ALPP, PTX3, PTPRC, PRKAR1A, PML, PLAUR, PLAT, PKM, SERPINA1, IL4, PRKN, SERPINE1, MSH2, MMP2, MLH1, MFAP1, MDM2, SMAD3, LIG4, LCAT, KRT10, ITGB3, ITGA2B, IL17A, MFT2
    • Bloom Syndrome Wikipedia
      Bloom syndrome Crystal structure of the Bloom's syndrome helicase BLM in complex with DNA (PDB ID: 4CGZ). Specialty Medical genetics Bloom syndrome (often abbreviated as BS in literature) [1] is a rare autosomal recessive genetic disorder characterized by short stature, predisposition to the development of cancer, and genomic instability. BS is caused by mutations in the BLM gene which is a member of the RecQ DNA helicase family. Mutations in other members of this family, namely WRN and RECQL4, are associated with the clinical entities Werner syndrome and Rothmund–Thomson syndrome , respectively. More broadly, Bloom syndrome is a member of a class of clinical entities that are characterized by chromosomal instability, genomic instability, or both and by cancer predisposition.
    • Bloom Syndrome GARD
      Bloom syndrome affects many different body systems and is characterized by slow growth, sun sensitivity, and an increased risk of cancer. Symptoms include short stature, sun-sensitive skin rash, and an immune system that doesn't work correctly. Some people with Bloom syndrome have learning disabilities, type 2 diabetes, and chronic obstructive pulmonary disease (COPD). Most people with Bloom syndrome develop some type of cancer by age 40. Bloom syndrome is caused by genetic variants in the BLM gene and is inherited in an autosomal recessive pattern.
    • Bloom Syndrome MedlinePlus
      Bloom syndrome is an inherited disorder characterized by short stature, a skin rash that develops after exposure to the sun, and a greatly increased risk of cancer. People with Bloom syndrome are usually smaller than 97 percent of the population in both height and weight from birth, and they rarely exceed 5 feet tall in adulthood. Affected individuals have skin that is sensitive to sun exposure, and they usually develop a butterfly-shaped patch of reddened skin across the nose and cheeks. A skin rash can also appear on other areas that are typically exposed to the sun, such as the back of the hands and the forearms. Small clusters of enlarged blood vessels (telangiectases) often appear in the rash; telangiectases can also occur in the eyes.
    • Bloom Syndrome OMIM
      A number sign (#) is used with this entry because Bloom syndrome (BLM), also referred to here as microcephaly, growth restriction, and increased sister chromatid exchange-1 (MGRISCE1), is caused by homozygous or compound heterozygous mutation in the gene encoding DNA helicase RecQ protein-like-3 (RECQL3; 604610) on chromosome 15q26. Description Bloom syndrome is an autosomal recessive disorder characterized by proportionate pre- and postnatal growth deficiency; sun-sensitive, telangiectatic, hypo- and hyperpigmented skin; predisposition to malignancy; and chromosomal instability. Genetic Heterogeneity of Microcephaly, Growth Restriction, and Increased Sister Chromatid Exchange See also MGRISCE2 (618097), caused by mutation in the TOP3A gene (601243) on chromosome 17p12. Clinical Features Landau et al. (1966) described a patient whose parents were second cousins and who showed low gamma-A and gamma-M serum proteins. German et al. (1984) collected information on 103 patients. German and Takebe (1989) suggested that differences in skin pigmentation in various ethnic groups may confer a degree of protection against actinic radiation and thus obscure one of the characteristic facial signs of Bloom syndrome, i.e., telangiectasia.
    • Bloom Syndrome Orphanet
      Bloom syndrome is a rare disorder associated with pre- and postnatal growth deficiency, a telangiectatic erythematous rash of the face and other sun-exposed areas, insulin resistance and predisposition to early onset and recurrent cancer of multiple organ systems. Epidemiology Bloom syndrome (BSyn) overall prevalence is unknown, but in the Ashkenazi Jewish population it is estimated at approximately 1/ 48,000 births. A founder mutation, known as BLM ash is present in approximately 1 in 100 persons of Ashkenazi Jewish background. There are also founder mutations in the Slavic and Hispanic populations. Clinical description Individuals with BSyn show proportionate growth deficiency of prenatal onset (average birth weight 1757 g) and continuing throughout life (average adult height of 149 cm for men and 138 cm for women).
  • Neuroendocrine Tumor Wikipedia
    Bronchial carcinoid can cause airway obstruction, pneumonia , pleurisy , difficulty with breathing, cough, and hemoptysis , or may be associated with weakness, nausea, weight loss, night sweats, neuralgia, and Cushing's syndrome.
    MEN1, CDKN1B, SSTR2, DAXX, ATRX, BRAF, TYMS, PTHLH, SSTR3, SSTR1, BAP1, MTOR, SST, GAST, SLC6A2, INSM1, CTNNB1, RET, PIK3CA, DNMT3A, POMC, EPHB1, PIK3CG, PIK3CD, CHGA, ELK3, CHEK2, PIK3CB, GRN, CD274, SMUG1, AKT1, GNA12, TP53, SYP, VEGFA, CDKN2A, ASCL1, BCL2, ENO2, NCAM1, GCG, MYCN, EGFR, MGMT, KIT, RASSF1, VHL, SCLC1, SSTR5, FOLH1, NKX2-1, KRAS, CALCA, CCND1, TAC1, PTPRF, VIP, NTS, PAX5, RHBDF2, GRP, IGF1, SDHD, GOT1, MAP2K7, CCK, ERBB2, DLL3, PPY, CXCL12, TP63, SMAD4, MUC1, INS, GCGR, CKAP4, NEUROD1, ISL1, MYC, NGF, SATB2, GLP1R, HSP90AA1, H3P10, HRAS, CHGB, CALR, NTRK1, TEK, DLK1, CDK4, CDX2, TGFA, UCHL1, RPE65, PGR, PDGFRA, CARTPT, CRH, UVRAG, SLC5A5, CXCR4, IGF1R, OTP, IL6, PHLDA3, TTF1, PAX8, TACR1, STK11, TRIM21, PLA2G15, SCG2, SQLE, SLC18A2, TERT, HDAC9, SLC2A1, PROM1, BCL2L11, NTSR1, PAX6, NAMPT, NOCT, INA, PLCB3, CD200, MKI67, PDX1, MAPK1, NES, HPSE, PTEN, STMN1, ABO, RIPK1, RORC, RAF1, IL1B, TRPV1, GATA3, ANGPT2, FOXM1, PTK2B, SDHAF2, ACCS, BDNF, EPAS1, EGF, ACSS2, MIB1, DNMT1, CCN2, TRPM8, CLDN4, CPE, CD34, CD44, FLNA, CEACAM5, B3GAT1, GH1, GIP, GHSR, GIPR, ADCY2, ALB, H3P28, TPPP2, H4C5, GGH, MIR1290, TMEM209, ELOA3, H4C13, H4C14, GPR151, SRPX, LGR5, TNFSF11, PSMG1, DCBLD2, H4-16, NRP1, MRGPRX4, SOCS1, H4C2, MIR3137, MRGPRX3, TNFRSF25, H3P12, CYYR1, AZIN2, DNER, AK6, MLIP, LMLN, NRP2, GPR68, MIR1246, H4C8, MAFK, MIR150, MIR155, MBOAT4, H4C9, MIR21, POTEKP, VN1R17P, SNORD95, GPR166P, ARID1A, EID3, SLC7A5, MIR375, H4C15, FZD4, MIRLET7C, OXER1, H4C12, HMGA2, H4C3, ARX, ELOA3B, GPRC6A, H4C11, H4C6, C17orf97, POTEM, MRGPRX1, ARMH1, H4C1, GADL1, ACTBL2, H4C4, BRI3, SQSTM1, ISYNA1, GHRL, ACOT7, KLF12, KRT20, SLC27A4, TET2, BCOR, EBNA1BP2, RALBP1, PGRMC1, LAMTOR1, FBXW7, MEG3, MAML3, TMEM127, NTNG1, ATRAID, KHDRBS1, DCTN4, SNORD61, NUP62, SNORD48, NTSR2, LPAR3, MAPK8IP2, SRRM2, BRD4, TRAM1, SPINK4, XIST, PPWD1, RBMS3, SETD1B, ZHX2, TNFSF13B, USE1, MAK16, UBE2Z, ONECUT2, FHL5, GCM2, DCLK1, ZBED1, ARHGEF2, PALB2, ALG9, SNED1, TET1, PDCD1LG2, TMPRSS13, MTA1, RPAIN, H1-10, EEF1E1, LGR6, PRMT5, NEUROD4, YAP1, SCML2, LANCL1, PAK4, RABEPK, ZNF197, CTNNBL1, PNO1, INSL5, EPB41L5, HDAC5, AKT3, CD302, GBA3, DCAF1, ATAT1, SERPINA3, VCL, CGA, ESR1, ERBB4, EPHB2, E2F1, DUSP2, DSG3, DPT, DPP4, DMBT1, DDC, DAD1, VCAN, CREB1, CRABP1, KLF6, CLU, FOXN3, CEACAM7, CEACAM3, ESR2, ETFA, EZH2, GHRH, HSPA4, AGFG1, HMOX1, HMGA1, GTF2H1, GSN, GNAS, GNA15, GFRA1, F3, GDNF, FSHR, FLT4, FLII, FLI1, FOXO1, FHIT, FGFR4, CGB3, CFL1, UQCRFS1, CDKN2C, FAS, APRT, APLP1, XIAP, APC, SLC25A6, SLC25A4, ANGPT1, ALK, AKT2, AFP, PARP1, ADCYAP1R1, ADCYAP1, ACVRL1, ACTN4, ACTG2, ACTG1, ACR, AQP4, ARF1, ATM, CASP3, CDK6, CD40LG, CD36, CD33, CCNE1, CCKBR, SERPINA6, CAV1, CA9, ATOH1, VPS51, C5, BRS3, BRCA2, DST, BAX, AVP, ATP4A, HTC2, HTR2A, TNC, IAPP, SDC1, SCT, SORT1, RNASE3, RARB, PTPRZ1, PTPRM, PTBP1, PSMD7, PSG2, PRKAR1A, PPP4C, POU4F1, PNN, PKD2, PITX2, PCYT1A, SERPINA5, PAX4, SDCBP, SDHB, SDHC, ST2, UBE2I, TPM3, TPH1, TNF, TM7SF2, TERC, TAT, STAT3, SSTR4, SEMA3F, SSR2, SOX11, SOX4, SOX2, SLPI, SLC3A2, SLC1A5, SFRP1, PAK3, PAK1, TNFRSF11B, KIF11, MDK, MAOA, LCN2, RPSA, L1CAM, KRT19, KRT7, KRT5, IL12A, MET, IL9, CXCL8, IL2, IL1A, IGFBP1, IGF2, IFNA13, IFNA1, MDM2, MFAP1, ODC1, MUTYH, NTRK2, NT5E, NRAS, NOTCH3, NPY, NOTCH1, NFKB1, NEFM, MUC4, CD99, NUDT1, COX2, MTAP, MST1R, MST1, MSMB, MMP7, MLH1, PTPRC
    • Neuroendocrine Tumors Mayo Clinic
      Overview Neuroendocrine tumors are cancers that begin in specialized cells called neuroendocrine cells. Neuroendocrine cells have traits similar to those of nerve cells and hormone-producing cells. Neuroendocrine tumors are rare and can occur anywhere in the body. Most neuroendocrine tumors occur in the lungs, appendix, small intestine, rectum and pancreas. There are many types of neuroendocrine tumors. Some grow slowly and some grow very quickly. Some neuroendocrine tumors produce excess hormones (functional neuroendocrine tumors).
  • Angina Wikipedia
    Other approaches include spinal cord stimulators, adenosine receptor blockade, and psychiatric intervention. [42] [43] [44] [45] [46] [47] Suspected angina [ edit ] Hospital admission for people with the following symptoms is recommended, as they may have unstable angina: pain at rest (which may occur at night), pain on minimal exertion, angina that seems to progress rapidly despite increasing medical treatment.
    AVP, PLAU, APOE, LDLR, GLA, CRELD1, ABCG8, ABCG5, GATA4, GATA6, XYLT2, XYLT1, NR2F2, LMNA, LCAT, JAK2, HLA-DPA1, HLA-DPB1, LDLRAP1, IDUA, LIPC, CYP27A1, TET2, PRTN3, ZMPSTE24, CTLA4, SCN5A, PTEN, MPL, ENPP1, PIGA, PCSK9, PTPN22, ABCC6, VEGFA, PMM2, APOB, ACE, CRP, CAD, CCS, IL6, SERPINE1, ITGB2, TNNI3, DLD, CXCL16, OXCT1, LAD1, SERPINA5, PLA2G1B, APOA1, TNF, NOS3, PLB1, KLF14, PLA2G7, PLA2G6, YWHAZ, IL37, NEAT1, VIP, MIR208A, MIR34A, MIR499A, TNFRSF1B, ZGLP1, CYP4F2, PROM1, TNFSF10, CPSF4, HDL3, MOCOS, QRSL1, POC1A, TBC1D9, JTB, ZC4H2, CMAS, SELL, EHMT1, PPP1R2C, FERMT3, ADIPOQ, WASF1, NLRP3, NR1I2, FGF21, ADAM10, CCL2, EDN1, ICAM1, HSPA5, GNB3, GLP1R, GLB1, GDF10, GCG, FGF4, F5, F3, CYP19A1, RENBP, CPB2, CLCN1, CETP, CD34, CD14, VPS51, KLK3, APOC3, ALB, AGTR1, IFNG, IGF2R, IL1A, IL1B, PYGM, PRKCD, PLXNA2, PLA2G2A, ABCB1, PAPPA, CNTN3, ADRB1, OPA1, NOS2, NOS1, MPI, MMP3, SMCP, LPA, KDR, ITGA2B, IL10, CXCL8, IL7, IL1RN, LINC02605
    • Angina Mayo Clinic
      Overview Angina (an-JIE-nuh or AN-juh-nuh) is a type of chest pain caused by reduced blood flow to the heart. Angina is a symptom of coronary artery disease. Angina is also called angina pectoris. Angina pain is often described as squeezing, pressure, heaviness, tightness or pain in the chest. It may feel like a heavy weight lying on the chest. Angina may be a new pain that needs to be checked by a health care provider, or recurring pain that goes away with treatment. Although angina is relatively common, it can still be hard to distinguish from other types of chest pain, such as the discomfort of indigestion.
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