Alagille syndrome

Alagille syndrome

*Gene map locus 20p12

AGS

AHD

AWS

Alagille-Watson syndrome

Arteriohepatic dysplasia

Bile ducts paucity, syndromic form

Cholestasis with peripheral pulmonary stenosis

Syndromatic hepatic ductular hypoplasia

[Clinical features: neonatal jaundice; characteristic facies; abnormalities of the liver, eyes, heart, and spine]

[Inheritance: autosomal dominant]

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NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway	NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway	Multiple Cerebral Aneurysms and Subarachnoid Hemorrhage in a Patient with Alagille Syndrome
American Journal of Human Genetics	American Journal of Human Genetics	American Journal of Neuroradiology


A 9-year-old Chinese boy with Alagille syndrome	A 9-year-old Chinese boy with Alagille syndrome	Vascular Anomalies in Alagille Syndrome: A Significant Cause of Morbidity and Mortality
Chinese Medical Journal	Chinese Medical Journal	Circulation


Alagille's Syndrome / Arteriohepatic Dysplasia - Elbow - Xanthomata	Alagille's Syndrome / Arteriohepatic Dysplasia - Palmar Hand - Xanthomata	Alagille's Syndrome / Arteriohepatic Dysplasia - Right elbow - Xanthomata
Department of Dermatology - University of Iowa	Department of Dermatology - University of Iowa	Department of Dermatology - University of Iowa


Mid aortic syndrome and Alagille syndrome	Mesangiolipidosis in Alagille syndrome - Relationship with apolipoprotein A-I	Abdominal Coarctation and Alagille Syndrome
Heart	Nephrology Dialysis Transplantation	Pediatrics


Abdominal Coarctation and Alagille Syndrome	Abdominal Coarctation and Alagille Syndrome	Moyamoya Syndrome in Children With Alagille Syndrome: Additional Evidence of a Vasculopathy
Pediatrics	Pediatrics	Pediatrics

18 images [ from 1 to 15 ]	1 2 next

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Edited by Aldo Campana, February 8, 2010