A case report : Alagille syndrome

Journal of the Medical Association of Thailand

Volumn 83, Issue 4, 2000, Pages 451-454

  Ukarapol, Nuthapong ^a   Wongsawasdi, Lumduan ^a   Sittiwangkul, Rekwan ^a  

^a Faculty of Medicine Chiang Mai University   (Thailand)

Author keywords

Alagille; Arteriohepatic Dysplasia; Cholestasis

Indexed keywords

ALAGILLE SYNDROME; ARTICLE; CASE REPORT; FEMALE; HUMAN; INFANT; PROGNOSIS; RISK ASSESSMENT;

ALAGILLE SYNDROME; FEMALE; HUMANS; INFANT; PROGNOSIS; RISK ASSESSMENT;

EID: 0034168793     PISSN: 01252208     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (3)

1. Watson GH, Miller V. Arteriohepatic dysplasia:familial pulmonary artery stenosis with neonatal liver disease. Arch Dis Child 1973;48:459-66.
2. Alagille D, Odievre M, Gautier M, Dommergues JP. Hepatic ductal hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental and sexual development, and cardiac murmur. J Pediatr 1975;86:63-71.
3. Hoffenberg EJ, Narkewicz MR, Sondheimer JM, Smith DJ, Silverman A, Sokol R. Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy. J Pediatr 1995;127:220-4.