Alagille's Syndrome A good, though brief (less than 1024 chars), description of your site. Psychosocial. Gastroenterology. arteriohepatic dysplasia OR ALAGILLE SYNDROME http://tray.dermatology.uiowa.edu/Alagil01.htm
Alagille Syndrome / The Family Village See also arteriohepatic dysplasia, WatsonAlagille Syndrome, Syndromic Hepatic Ductular Hypoplasia, Syndromic http://www.familyvillage.wisc.edu/lib_alag.htm
Extractions: See also: Arteriohepatic Dysplasia, Watson-Alagille Syndrome, Syndromic Hepatic Ductular Hypoplasia, Syndromic Intrahepatic Biliary Hypoplasia, Cholestasis with Peripheral Pulmonary Stenosis, Syndromic Bile Duct Paucity, Intrahepatic Biliary Artresia or Dysgenesis. ASA's mission is to provide information about Alagille syndrome, networking services, and a forum for exchange of experiences for families with the syndrome. They also disseminate information to all those interested in this rare liver disorder, and will refer families to others in the same geographical area. The Alliance publishes a quarterly newsletter, LiverLinks , and has a brochure and a fact sheet available that explain the syndrome and treatment that is available. ASA offers a new parent packet that includes, the newsletter, fact sheet, brochure, and an information form for referrals. ASA collects information on physicians and research being done and makes this information available to its members on a limited basis. They are in the process of developing a bibliography of articles and they have a scientific advisory board.
Alagille's Syndrome (www.whonamedit.com) G. H. Watson, V. Miller arteriohepatic dysplasia. Familial pulmonary artery stenosis with neonatal liver disease. http://www.whonamedit.com/synd.cfm/729.html
Extractions: Arterio-hepatic dysplasia, cardiovertebral syndrome, cholestasis-peripheral pulmonary stenosis, cholestasis-pulmonary artery stenosis, cholestasis with peripheral pulmonary stenosis, hepatic ductular hypoplasia, hepatic ductal hypoplasia-multiple malformations syndrome, hepatofacial-neurocardiac-vertebral syndrome, cholestasis-pulmonary artery stenosis syndrome, hepatofacioneurocardiovertebral syndrome, paucity of interlobular ducts. A congenital familial syndrome with onset during first three months of life, affecting both sexes. Marked by clinical picture with intrahepatic cholestasis due to hypoplasia of the interlobular biliary duct, neonatal jaundice, hepatomegaly (from 3rd month). Long list of symptoms include dysmorphic (flat) facies sometimes referred to as cholestasis facies, with prominent forehead, mongoloid slant, mild hypertelorism, straight or bulbous nose, and skeletal anomalies; occasionally diffuse xanthomas (palms, extensor areas, creases), and pruritus, Harsh mesosystolic murmur. Growth and mental retardation. In males, hypogonadism. Etiology unknown. Inheritance is autosomal dominant with reduced penetrance and variable expressivity.
Gastroenterology - Alagille Syndrome Gastroenterology. arteriohepatic dysplasia OR ALAGILLE SYNDROME. Alagillefirst described a syndrome consisting of a paucity of interlobular http://www.mc.vanderbilt.edu/peds/pidl/gi/alagille.htm
Extractions: PIDL Home/ Contents Development Nutrition Acute Illness ... Psychosocial Gastroenterology ARTERIOHEPATIC DYSPLASIA OR ALAGILLE SYNDROME Alagille first described a syndrome consisting of a paucity of interlobular bile ducts with chronic cholestasis. Patients with this syndrome typically have the following major features: peculiar facies, chronic cholestasis, butterfly- like vertebral arch defects, and peripheral pulmonary artery hypoplasia or stenosis, either isolated or associated with complex cardiovascular abnormalities. Other less frequent features include growth retardation, mental retardation, renal disturbances, other vascular malformations, high- pitched voice, and delayed puberty with hypogonadism. Patients typically present with conjugated hyperbilirubinemia from chronic cholestasis within the first 3 months of life. Hepatomegaly and splenomegaly are almost invariably present. A remarkable feature is the extreme degree of pruritus. The splenomegaly may actually precede the development of portal hypertension. Xanthomas are commonly seen on the extensor surfaces of the fingers, palmar creases, nape of the neck, anal folds, popliteal fossa, and inguinal area. There is marked elevation of cholesterol, phospholipid, and triglyceride levels. Typically liver enzymes are found to be normal.
Alagille Syndrome(arteriohepatic Dysplasia) Alagille syndrome(arteriohepatic dysplasia). the the most common syndrome incorporatingintrahepatic bile duct paucity. progressive destruction of bile ducts. http://www.vghtc.gov.tw:8082/ped/teaching/inout/alagille syndrome/tsld002.htm
Alagille's Syndrome - 3 Dacri, dacrio-, dacria / Dacry-, dacryo-, dacry Componentes iniciales y final de las voces castellanas que denotan relación con las lágrimas. Dacriadenalgia / Dacryadenalgia Dacriadenectomía / Dacryadenectomy Dacriadenitis / Dacryadenitis http://tray.dermatology.uiowa.edu/Alagil03.htm
Alagille Syndrome(arteriohepatic Dysplasia) The summary for this Chinese (Traditional) page contains characters that cannot be correctly displayed in this language/character set. http://www.vghtc.gov.tw:8082/ped/teaching/inout/alagille syndrome/sld002.htm
Extractions: Chromosome Entry Maps with Pix. Known Disease Entitys Entry Map # Title MIM # Disorders Bone morphogenetic protein-2 ?Fibrodysplasia ossificans progressiva (1) Phosphoenolpyruvate carboxykinase-1 (soluble) ?Hypoglycemia due to PCK1 deficiency (1) Growth hormone releasing factor; somatocrinin ?Isolated growth hormone deficiency , Gigantism due to GHRF hypersecretion (1) Inosine triphosphatase-A [Inosine triphosphatase deficiency] (1) Alagille syndrome (arteriohepatic dysplasia) Alagille syndrome (2) Cystatin C Cerebral amyloid angiopathy (3) Congenital hereditary endothelial dystrophy of cornea Congenital hereditary endothelial dystrophy of cornea Posterior polymorphous corneal dystrophy Corneal dystrophy, posterior polymorphous (2) Prion protein (p27-30) Creutzfeldt-Jakob disease, 123400 (3); Insomnia, fatal familial (3) Arginine vasopressin (neurophysin II, antidiuretic hormone) Diabetes insipidus, neurohypophyseal, 125700 (3) Cholinergic receptor, nicotinic, alpha polypeptide-4 Epilepsy, benign neonatal, type 1, (3); Epilepsy, frontal lobe Protective protein for beta-galactosidase (cathepsin A) Galactosialidosis (3) Glutathione synthetase Hemolytic anemia due to glutathione synthetase Transcription factor 14, hepatic nuclear factor (HNF4)
University Of Miami School Of Medicine - Glossary - Alagille Syndrome Alagille syndrome Also known as arteriohepatic dysplasia, this is a genetic disordercharacterized by jaundice in the newborn period, liver disease with http://www.med.miami.edu/patients/glossary/art.asp?articlekey=6752
Wipro GE Medical Biliary atresia. c. arteriohepatic dysplasia (Alagille's syndrome). d. http://www.wipro-ge.com/ultrasound/quiz/quiz_archive_blk2q3.html
Arteriohepatic Dysplasia - General Practice Notebook medical information from General Practice Notebook. arteriohepatic dysplasia. Alagillesyndrome is defined clinically as the combination of biliary hypoplasia; http://www.gpnotebook.co.uk/cache/-644218858.htm
Sitemap Of GPnotebook.co.uk cell crises of the lung / hypostatis dermatitis / vertebrosternal ribs / monocyticleukaemia / white pimples / arteriohepatic dysplasia / pigmentation(linear http://www.gpnotebook.co.uk/sitemap17.htm
Abnormalities, Multiple ALAGILLE SYNDROME; AGS; Alagille Syndrome Amer. Liver Found. Alagille's Syndrome/ arteriohepatic dysplasia Back (Date 10/1980) - Xanthomata U. of Iowa; http://www.ohsu.edu/cliniweb/C16/C16.131.77.html
