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  • Aleutian Disease Wikipedia
    . ^ ELIMINATION OF PATHOGENIC INFECTION IN FARMED ANIMAL POPULATIONS ^ Canuti M, O'Leary KE, Hunter BD, Spearman G, Ojkic D, Whitney HG, Lang AS (January 2016).
    PTPN11, IVNS1ABP
  • Ear Mite Wikipedia
    PMID 17488924 . ^ Klemm, E; Haroske, G; Wollina, U (2009). "Otitis externa and myringitis due to demodicidosis" (PDF) .
  • Inclusion Body Disease Wikipedia
    ., Sanders, C., Kistler, A. L., Ruby, J. G., Franco, J. Y., Reavil, D. R., Dunker, F and DeRisi.
  • Aminolevulinic Acid Dehydratase Deficiency Porphyria Wikipedia
    ISBN 978-1-4160-2999-1 . ^ a b c d e f g h i j k l m n o "ALAD-Deficiency Porphyria (ADP)" .
    ALAD, HMBS, CPOX, FECH, UROD, CYP2B6, PPOX
    • Hepatic Porphyria Wikipedia
      Hepatic porphyria Specialty Endocrinology Hepatic porphyrias is a form of porphyria in which toxic porphyrin molecules build up in the liver . Hepatic porphyrias can result from a number of different enzyme defiencies. [1] Examples include (in order of synthesis pathway): Acute intermittent porphyria Porphyria cutanea tarda and Hepatoerythropoietic porphyria Hereditary coproporphyria Variegate porphyria See also [ edit ] Erythropoietic porphyria References [ edit ] ^ "OMIM - PORPHYRIA, CONGENITAL ERYTHROPOIETIC" . Retrieved 2008-12-04 . External links [ edit ] Classification D ICD - 10 : E80 ICD - 9-CM : 277.1 MeSH : D017094 Porphyrias,+Hepatic at the US National Library of Medicine Medical Subject Headings (MeSH) www.drugs-porphyria.com www.porphyria-europe.com v t e Heme metabolism disorders Porphyria , hepatic and erythropoietic ( porphyrin ) early mitochondrial: ALAD porphyria Acute intermittent porphyria cytoplasmic: Gunther disease/congenital erythropoietic porphyria Porphyria cutanea tarda / Hepatoerythropoietic porphyria late mitochondrial: Hereditary coproporphyria Harderoporphyria Variegate porphyria Erythropoietic protoporphyria Hereditary hyperbilirubinemia ( bilirubin ) unconjugated: Gilbert's syndrome Crigler–Najjar syndrome Lucey–Driscoll syndrome conjugated: Dubin–Johnson syndrome nd sheet Rotor syndrome This article about an endocrine, nutritional, or metabolic disease is a stub . You can help Wikipedia by expanding it . v t e
  • Caustic Ingestion Wikipedia
    Caustic ingestions in adults usually involve larger amounts of ingested material during attempts of self harm. [1] Due to the greater amount of material usually ingested; injuries are often more severe in the intentional ingestions of adolescents and adults as compared to those of children. [1] Commonly ingested substances include ammonium hydroxide (found in general cleaner and grease remover), sodium hydroxide or potassium hydroxide (found in drain opener or oven cleaner), sodium hypochlorite (bleach), oxalic acid (metal polish) and hydrochloric acid (toilet bowl cleaner). [1] Storage of caustic substances in water or drink containers is a risk factor for accidental ingestion of these materials, particularly in children. [2] Boys of preschool age are at the greatest risk of accidental caustic ingestion. [3] Prevention [ edit ] Preventative measures have been recommended that are intended to decrease the risk of accidental ingestion of caustic substances including": [3] Keeping caustic substances in locked cabinets or on upper shelves Not storing chemical substances in food or drink containers Not keeping large amounts of detergent in the home Not mentioning a drug as "candy" when giving it as medication Keeping the phone number for poison control in the home Keeping caustic substances in labelled containers References [ edit ] ^ a b c d e f g h i j k l m n o p q r s Longo, Dan L.; Hoffman, Robert S.; Burns, Michele M.; Gosselin, Sophie (30 April 2020).
  • Sphingolipidoses Wikipedia
    .; Kampmann, C.; Linhart, A.; Sunder-Plassmann, G.; Ries, M.; Beck, M. (2004). "Fabry disease defined: Baseline clinical manifestations of 366 patients in the Fabry Outcome Survey".
    PSAP, SMPD1, SGPL1, NR0B1, POLE, OGA, BECN1, STAR, NPC1, ARSA, HSPA4, GLB1, NR5A1, CYP11A1, CDKN1C, ATP2A3, SAMD9
  • Persistent Thyroglossal Duct Wikipedia
    The Sistrunk procedure has a reoccurrence rate of less than 5%, proving it is extremely effective at removing the majority of traces of the persistent thyroglossal duct. [6] References [ edit ] ^ Kurt A, Ortug C, Aydar Y, Ortug G (April 2007). "An incidence study on thyroglossal duct cysts in adults".
  • Aseptic Meningitis Wikipedia
    Retrieved 20 April 2018 . ^ a b c d e f g h Irani DN (August 2008). "Aseptic meningitis and viral myelitis" .
    IL6, ALB, NR4A3, CHN1, CSF2, LAMC2, CNOT7, CHAF1A, CNOT8, CHAF1B, MOG, TPI1, MRC1, APEX1, CXCL8, ACE, LRG1
  • Orf (Disease) Wikipedia
    A veterinarian must be contacted if there is a risk of misdiagnosis with other, more serious conditions. [1] See also [ edit ] Ecthyma List of cutaneous conditions List of immunofluorescence findings for autoimmune bullous conditions References [ edit ] ^ a b c d e f g Winter, Agnes; Charmley, Judith (1999).
    COL6A2, SLC26A4
  • Hemarthrosis Wikipedia
    PMID 21901684 . ^ Goldberg A, Stansby G "Surgical Talk" 2nd edition External links [ edit ] Classification D ICD - 10 : M25.0 ICD - 9-CM : 719.1 MeSH : D006395 DiseasesDB : 29653 v t e Diseases of joints General Arthritis Monoarthritis Oligoarthritis Polyarthritis Symptoms Joint pain Joint stiffness Inflammatory Infectious Septic arthritis Tuberculosis arthritis Crystal Chondrocalcinosis CPPD (Psudogout) Gout Seronegative Reactive arthritis Psoriatic arthritis Ankylosing spondylitis Other Juvenile idiopathic arthritis Rheumatoid arthritis Felty's syndrome Palindromic rheumatism Adult-onset Still's disease Noninflammatory Hemarthrosis Osteoarthritis Heberden's node Bouchard's nodes Osteophyte v t e Disorders of bleeding and clotting Coagulation · coagulopathy · Bleeding diathesis Clotting By cause Clotting factors Antithrombin III deficiency Protein C deficiency Activated protein C resistance Protein S deficiency Factor V Leiden Prothrombin G20210A Platelets Sticky platelet syndrome Thrombocytosis Essential thrombocythemia DIC Purpura fulminans Antiphospholipid syndrome Clots Thrombophilia Thrombus Thrombosis Virchow's triad Trousseau sign of malignancy By site Deep vein thrombosis Bancroft's sign Homans sign Lisker's sign Louvel's sign Lowenberg's sign Peabody's sign Pratt's sign Rose's sign Pulmonary embolism Renal vein thrombosis Bleeding By cause Thrombocytopenia Thrombocytopenic purpura : ITP Evans syndrome TM TTP Upshaw–Schulman syndrome Heparin-induced thrombocytopenia May–Hegglin anomaly Platelet function adhesion Bernard–Soulier syndrome aggregation Glanzmann's thrombasthenia platelet storage pool deficiency Hermansky–Pudlak syndrome Gray platelet syndrome Clotting factor Hemophilia A/VIII B/IX C/XI von Willebrand disease Hypoprothrombinemia/II Factor VII deficiency Factor X deficiency Factor XII deficiency Factor XIII deficiency Dysfibrinogenemia Congenital afibrinogenemia Signs and symptoms Bleeding Bruise Hematoma Petechia Purpura Nonthrombocytopenic purpura By site head Epistaxis Hemoptysis Intracranial hemorrhage Hyphema Subconjunctival hemorrhage torso Hemothorax Hemopericardium Pulmonary hematoma abdomen Gastrointestinal bleeding Hemobilia Hemoperitoneum Hematocele Hematosalpinx joint Hemarthrosis
    F2, F7, F8, F9, F10, F11, F13A1, F13B, GGCX, PLAU, SERPINF2, VWF, WAS
  • Sertoli–leydig Cell Tumour Wikipedia
    External links [ edit ] Media related to Sertoli–Leydig cell tumors at Wikimedia Commons Classification D ICD - 9-CM : 183.0 , 256.1 ICD-O : 8630-8631/0 MeSH : D018310 External resources MedlinePlus : 001172 v t e Tumors of the female urogenital system Adnexa Ovaries Glandular and epithelial / surface epithelial- stromal tumor CMS: Ovarian serous cystadenoma Mucinous cystadenoma Cystadenocarcinoma Papillary serous cystadenocarcinoma Krukenberg tumor Endometrioid tumor Clear-cell ovarian carcinoma Brenner tumour Sex cord–gonadal stromal Leydig cell tumour Sertoli cell tumour Sertoli–Leydig cell tumour Thecoma Granulosa cell tumour Luteoma Sex cord tumour with annular tubules Germ cell Dysgerminoma Nongerminomatous Embryonal carcinoma Endodermal sinus tumor Gonadoblastoma Teratoma / Struma ovarii Choriocarcinoma Fibroma Meigs' syndrome Fallopian tube Adenomatoid tumor Uterus Myometrium Uterine fibroids/leiomyoma Leiomyosarcoma Adenomyoma Endometrium Endometrioid tumor Uterine papillary serous carcinoma Endometrial intraepithelial neoplasia Uterine clear-cell carcinoma Cervix Cervical intraepithelial neoplasia Clear-cell carcinoma SCC Glassy cell carcinoma Villoglandular adenocarcinoma Placenta Choriocarcinoma Gestational trophoblastic disease General Uterine sarcoma Mixed Müllerian tumor Vagina Squamous-cell carcinoma of the vagina Botryoid rhabdomyosarcoma Clear-cell adenocarcinoma of the vagina Vaginal intraepithelial neoplasia Vaginal cysts Vulva SCC Melanoma Papillary hidradenoma Extramammary Paget's disease Vulvar intraepithelial neoplasia Bartholin gland carcinoma v t e Tumors of the male urogenital system Testicles Sex cord– gonadal stromal Sertoli–Leydig cell tumour Sertoli cell tumour Leydig cell tumour Germ cell G Seminoma Spermatocytic tumor Germ cell neoplasia in situ NG Embryonal carcinoma Endodermal sinus tumor Gonadoblastoma Teratoma Choriocarcinoma Embryoma Prostate Adenocarcinoma High-grade prostatic intraepithelial neoplasia HGPIN Small-cell carcinoma Transitional cell carcinoma Penis Carcinoma Extramammary Paget's disease Bowen's disease Bowenoid papulosis Erythroplasia of Queyrat Hirsuties coronae glandis
  • Spinal Fracture Wikipedia
    CS1 maint: multiple names: authors list ( link ) ^ Saragiotto, Bruno T; Maher, Christopher G; Lin, Chung-Wei Christine; Verhagen, Arianne P; Goergen, Stacy; Michaleff, Zoe A (2018).
  • Melanocytoma Wikipedia
    PMID 12207136 (Review). ^ a b Timothy Murray, Timothy G. (2010). "Clinical imaging and high-resolution ultrasonography in melanocytoma management" .
  • Pachychoroid Disorders Of The Macula Wikipedia
    . ^ a b Siedlecki, Jakob; Schworm, Benedikt; Priglinger, Siegfried G. (December 2019). "The Pachychoroid Disease Spectrum—and the Need for a Uniform Classification System".
  • Cytoplasmic Male Sterility Wikipedia
    . ^ Tuteja R, Saxena RK, Davila J, Shah T, Chen W, Xiao YL, Fan G, Saxena KB, Alverson AJ, Spillane C, Town C, Varshney RK (October 2013).
  • Trisomy 22 Wikipedia
    This condition has several different names: 22q11.2 deletion syndrome, Velocardiofacial syndrome, DiGeorge syndrome, conotruncal anomaly face syndrome, Opitz G/BBB syndrome, and Cayler cardiofacial syndrome.
    FLT3, KIT, MYH11, PML, CHDH
    • Trisomy 22 GARD
      Trisomy 22 is a chromosome disorder in which an extra (third) copy of chromosome 22 is present in every cell of the body where there should normally only be two copies. This condition is commonly found in miscarriages, but only rarely in liveborn infants. Most affected individuals die shortly before or shortly after birth due to severe complications. Common features include an underdeveloped midface (midface hypoplasia) with flat/broad nasal bridge, malformed ears with pits or tags, cleft palate, hypertelorism (wide-spaced eyes), microcephaly and other cranial abnormalities, congenital heart disease , genital abnormalities, and intrauterine growth restriction (IUGR).
  • Petechia Wikipedia
    Sunburn, childbirth, weightlifting [3] Gua Sha , a Chinese treatment that scrapes the skin High-G training Hickey Asphyxiation Choking game Oral sex [4] Non-infectious conditions [ edit ] Vitamin C deficiency, scurvy [3] Vitamin K deficiency [3] Leukemia [3] Thrombocytopenia – Low platelet counts or diminished platelet function (e.g., as a side effect of medications or during certain infections) can give rise to petechial spots [1] clotting factor deficiencies – ( Von Willebrand disease ) Hypocalcemia Idiopathic thrombocytopenic purpura Coeliac disease Aplastic anaemia Lupus Kwashiorkor or Marasmus – Childhood protein-energy malnutrition Erythroblastosis fetalis Henoch–Schönlein purpura Kawasaki disease Schamberg disease Ehlers–Danlos syndrome Sjögren syndrome – Petechial spots could occur due to vasculitis , an inflammation of the blood vessels.
    ADAMTS13, IFIH1, F11, HLA-DRB1, IL10, JAK2, LYZ, TNF, KLK4, ADRM1, RBM45
  • Parinaud's Syndrome Wikipedia
    Further reading [ edit ] Aguilar-Rebolledo F, Zárate-Moysén A, Quintana-Roldán G (1998). "Parinaud's syndrome in children".
  • Fragmentation Of Memory Wikipedia
    CA: Wadsworth Publishing. pp. 191–192. ^ Bartram, G. (2008). "Memory, Amnesia and Identity in Hermann Broch's Schlafwandler Trilogy".
  • Maternal Near Miss Wikipedia
    Identification criteria [ edit ] According to the World Health Organization, if a woman presents any of the conditions below during pregnancy, childbirth or within 42 days of termination of pregnancy and survives, she is considered as a maternal near miss case. [10] Cardiovascular dysfunction a) Shock b) Cardiac Arrest c) Severe hypoperfusion (lactate >5 mmol/L or >45 mg/dL) d) Severe acidosis (pH<7.1) e) Use of continuous vasoactive drugs f) Cardio-pulmonary resuscitation Respiratory dysfunction g) Acute cyanosis h) Gasping i) Severe tachypnea (respiratory rate>40 breaths per minute) j) Severe bradypnea (respiratory rate<6 breaths per minute) k) Severe hypoxemia (O2 saturation <90% for ≥60min or PAO2/FiO2<200) l) Intubation and ventilation not related to anaesthesia Renal dysfunction m) Oliguria non responsive to fluids or diuretics n) Severe acute azotemia (creatinine >300 μmol/ml or >3.5 mg/dL) o) Dialysis for acute renal failure Coagulation dysfunction p) Failure to form clots q) Severe acute thrombocytopenia (<50,000 platelets/ml) r) Massive transfusion of blood or red cells (≥ 5 units) Hepatic dysfunction s) Jaundice in the presence of pre-eclampsia t) Severe acute hyperbilirubinemia (bilirubin>100 μmol/L or >6.0 mg/dL) Neurologic dysfunction u) Prolonged unconsciousness or coma (lasting >12 hours) v) Stroke w) Uncontrollable fit / status epilepticus x) Global paralysis Uterine dysfunction y) Hysterectomy due to uterine infection or haemorrhage Sources [ edit ] Adisasmita, Asri; et al. (2008).
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