Alagille syndrome in children

Alagille syndrome in children

Alagill syndrome is a rare genetic disease with an autosomal dominant type of inheritance, which is characterized by chronic intrahepatic cholestasis due to an abnormality of the biliary tree in combination with multiple malformations. It presents certain difficulties in diagnosing little children,...

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Bibliographic Details
Main Authors:	G. V. Volynets, A. V. Nikitin, T. A. Skvortsova
Format:	Article
Language:	Russian
Published:	Ltd. “The National Academy of Pediatric Science and Innovation” 2020-05-01
Series:	Rossijskij Vestnik Perinatologii i Pediatrii
Subjects:	children, chronic intrahepatic cholestasis, alagille syndrome
Online Access:	https://www.ped-perinatology.ru/jour/article/view/1118

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