The EOPS Source Index 1991 9148 Jensen O A Alagille s syndrome (arteriohepatic dysplasia) hepatocellular carcinoma associated with the syndrome in a 4- year old girl 91-49 Stefani FH http://www.helsinki.fi/laak/silk/perus/EOPS1991.html
Extractions: Go to Home Previous Next 60's ... Notes Jakobiec F A Adult extra-renal rhabdoid tumor of the lacrimal gland Hidayat A A Congenital malignant rhabdoid tumor of the eye and orbit Garner A Lacrimal gland myoepithelioma Friedman A H Fibrous histiocytoma of the lacrimal sac Lee W R Malignant fibrous histiocytoma of orbit: infarction of optic nerve Kock E Chondroma of the orbit Font R L Recurrent well differentiated orbital liposarcoma with myxoid areas occurring in a teenager Tarkkanen A Malignant fibrous histiocytoma of the orbit with spontaneous resolution Latkovic Z Orbital carcinoma of unknown origin - a case for diagnosis Prause J U Castleman's disease in one orbit Goder G J Kimura's disease of the orbit McLean I Primary histiocytoid carcinoma of the eyelid Boniuk M Unusual bluish tumors of the eyelid and conjunctiva: angioleiomyoma and glomangioma Sterkers M An atypical case of tumour of the eyebrow: melanoma or sarcoma? Mullaney J Conjunctival nodule with testicular tumour Conjunctival malignant melanoma Frayer W C Granulomatous conjunctivitis Ferry A P Teddy bear granuloma of conjunctiva (synthetic fiber granuloma) Manschot W A Not-predictable melanoma reaction on empirical radiation doses Naeser P Proton beam treated malignant melanoma Crawford J B Spindle cell tumor of eyelid in patient with lymphoma de Wolff-Rouendaal D Ciliary body and iris metastasis of cutaneous melanoma in a patient with dysplastic naevus syndrome Albert D M Hepatoblastoma metastatic to the eye
English/ Español arteriohepatic dysplasia. Definition arteriohepatic dysplasia is a genetic disorder that mimics other forms of prolonged liver disease http://stagnes.cht-info.com/Library/onelibrary.cfm?id=766
MUMS List Of Disorders - A Syndrome (1); ArnoldChiari Syndrome w/Spina Bifida (22) *; arteriohepatic dysplasia (AHD) (Alagille Syndrome) (12) *; Arteriosclerosis (3 http://www.netnet.net/mums/mum_a.htm
Extractions: indicates there is a support group which covers that diagnosis. 2 Hydroxic Gluteric Urea (1) 2 Keto Adepic Aciduria (1) 3 Hydroxy 3-Methylglutaryl CoAlyase Deficiency (HMG) (1) * 3 Methycrotonyl CoA Carboxylase Deficiency (3MCCC) (1) 3 Methylglutaconic Aciduria (4) 4 Hydroxybutyric Aciduria (1) 4A Syndrome(Adrenocortical Insufficiency, Alacrima, Achalasia,Autonomic)(1) 5 Alpha Reductase Deficiency (1) * 5 Oxoprolinuria (Pyroglutamic Aciduria) (1) 18 Hydroxylase Deficiency (Adrenal Hyperplasia) (1) 21 Hydroxylase Deficiency (Adrenal Hyperplasia) (18) ** ACTH Deficiency (1) AIDS (Acquired Immune Deficiency Syndrome) (6) ** Aarskog Syndrome (8) ** Abdominal Chylous Ascites (abdomen fills w/fluid) (4) Abdominal Migraines (2) Abdominal Teratoma Tumor (5) Abetalipoproteinemia (4) * Abetalipoproteinemia (Bassen-Kornzweig Syndrome) (1) * Absence of Arm Below Elbow, Congenital (25) * Absence of Arms (Severed in accident) (2) * Absence of Arms, Hands attached to shoulder (1) *
The World Diseases A 2 Z Names By Countrylinks And Dr Impex Aphasia. Aplastic Anemia. Apnea, Sleep. Appendicitis. Arrhythmia. arteriohepatic dysplasia. Arthritis. Arthrogryposis. Asbestosis. Asperger s Syndrome. Aspergillosis. http://www.countrylinks.biz/diseases.htm
Karger Publishers chromosome 20 are rare and most cases of short arm deletions of this chromosome are associated with the main signs of arteriohepatic dysplasia (AlagilleWatson http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=
Medical Information Site With Residency Directory, Auctions, Lab Right Ventricular Cardiomyopathy 207) Arrhythmogenic Right Ventricular Dysplasia 208) Arsenic Poisoning 209) arteriohepatic dysplasia 210) Arteriosclerosis 211 http://www.residency.info/dxenc/index.php?v=2&l=A
Transplantation | Children's Hospital & Regional Medical Center and others; Alpha1-antitrypsin deficiency; arteriohepatic dysplasia (Alagille syndrome); Biliary and gall bladder disorders; Biliary http://www.seattlechildrens.org/our_services/clinical_services/transplantation.a
Extractions: Seattle, WA You are here: Home Our Services Clinical Services Text size: Normal Large Children's Hospital and Regional Medical Center offers transplantation programs for heart, liver, kidney and bone marrow. We evaluate patients for surgery and manage the disease before transplant. We provide transplant surgery and vital follow-up care. Skilled teams of health-care professionals focus on the needs of our patients. We also attend to their families' support needs. Pediatric transplantation is the accepted treatment of choice for end-stage organ disease in children. Transplantation can provide patients with an improved quality of life. We give our pediatric transplant candidates and their families assistance preparing for organ transplantation. This may include physical, emotional and financial support. Our staff members are specialists in pediatric organ transplantation. The transplant service is a primary affiliate of the Division of Transplantation, University of Washington Department of Surgery.
Healthcyclopedia Index - A Aphasia, Aplastic Anemia. Apnea, Sleep, Appendicitis. Arrhythmia, arteriohepatic dysplasia. Arthritis, Arthrogryposis. Asbestosis, Asperger s Syndrome. http://www.healthcyclopedia.com/a.html
Cloned Lambs[ 151]lessons From Pathology 2c,d online) are also seen in the rare congenital human diseases bile duct atresia (not identified here) and the Alagille syndrome (arteriohepatic dysplasia) 8 http://www.nature.com/cgi-taf/DynaPage.taf?file=/nbt/journal/v21/n7/full/nbt0703
Alagille Syndrome disorder subdivision(s) covered by this report. Synonyms AHD; arteriohepatic dysplasia; Cholestasis with Peripheral Pulmonary Stenosis; http://my.webmd.com/hw/health_guide_atoz/nord473.asp
Extractions: Alagille Syndrome is a genetic liver disorder usually present at birth. It is characterized by insufficient passage of bile due to a lower than normal number of bile ducts inside the liver. In some cases, the child may be born with no bile ducts. Major symptoms include prolonged yellow skin discoloration (jaundice), eye and heart structure anomalies, abnormally shaped vertebrae of the spine, compression of nerve space inside the lower spine, an absence of deep tendon reflexes, mental deficiency, facial and kidney (renal) abnormalities, shortened fingers, and pancreatic insufficiency.
Index Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Arrhythmogenic Right Ventricular Dysplasia (ARVD) ARSA arteriohepatic dysplasia Arteriosclerosis, Retina http://my.webmd.com/hw/index/index-topics-A.asp
Alagille Syndrome Notes for physicians on Alagille Syndrome (arteriohepatic dysplasia, AHD) covering diagnosis, clinical description, differential diagnosis, management http://omni.ac.uk/browse/mesh/C0085280L0085513.html
Extractions: low graphics broader: Abnormalities, Multiple other: Angelman Syndrome Beckwith-Wiedemann Syndrome Branchio-Oto-Renal Syndrome Cockayne Syndrome ... GeneReviews : Alagille Syndrome Notes for physicians on Alagille Syndrome (Arteriohepatic Dysplasia, AHD) covering diagnosis, clinical description, differential diagnosis, management, molecular genetics and genetic counselling. Revised during May 2000, this resource forms part of GeneReviews (formerly GeneClinics profile), a peer-reviewed clinical genetic information resource that is funded by the US National Institutes of Health (NIH) and produced by the University of Washington, Seattle. This resource contains a summary and bibliographical references of the review, free access to the full-text version of the review requires brief registration. Alagille Syndrome / genetics
Terminology - Medical Transcription At Medword Dyspepsia Dyspeptic Dysphagia Dysphonia, spasmodic Dysphoria dysplasia dysplasia, arteriohepatic dysplasia, bronchopulmonary dysplasia http://www.medword.com/medterms_dTEXT.html
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Extractions: Interlobulaarinen sappitiehyeiden harvalukuisuus Oireyhtymällä tarkoitetaan sappitiehyiden harvalukuisuuden aiheuttamaa sapensalpausta yhdistyneenä sydän- ja verisuoni- sekä muihin epämuodostumiin. Sen päätunnusmerkkeihin kuuluvat otsan kohoutuminen, syvälle asettuneet ja etäällä toisistaan sijaitsevat silmät, suora nenä ja suippo leuka, toisinaan myös käheä ääni ja muitakin epänormaaleja piirteitä. Keskitasoista kehitysvammaisuutta esiintyy noin 15 %:lla. Yläleuan hampaat saattavat olla eteen työntyneet ja korvat esinipistävät. Silmien verkkokalvojen väriaine voi olla epätasaisesti jakautunut ja karsastusta saattaa esiintyä, samoin näköhermon nystyn poikkeavuutta ja pupillien virheellistä sijoittumista (silmävikoja 78 %:lla). Nenän kärki on usein sipulimainen. Oireyhtymään kuuluvat myös nikamankaaren vauriot (51 %:lla), nikaman keskiosan puuttuminen, puolinikamaisuus ja nikamien yhteensulautuminen, lannenikamien etäistyminen, vartalon ja kasvojen ihon verisuoniston laajentumisen aiheuttamat läiskät ja kämmenien punoitus, ihokarvoituksen niukkuus, heikentyneet refleksit, sydämen sivuäänet (97 %:lla), keuhkovaltimon ahtauma, sydämen väliseinävauriot, kehittymätön aortta
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