Alagille syndrome with unusual common bile duct hypoplasia and gallbladder dysmorphism: Lesson based on a case report

Alagille syndrome is an autosomal dominant and multisystemic disease that generally manifests itself with intrahepatic bile ducts paucity, chronic cholestasis, xanthomas and with other less frequent clinical manifestations such as congenital heart disease, skeletal abnomalies, ophthalmic, vascular,...

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Auteurs principaux:	Renato Farina, MD, Alfredo Garofalo, MD, Pietro Valerio Foti, PhD, Corrado Inì, MD, Claudia Motta, MD, Sebastiano Galioto, MD, Mariangela Clemenza, MD, Adriana Ilardi, MD, Livio Gavazzi, MD, Daniele Grippaldi, MD, Mattia D'Urso, MD, Antonio Basile, PhD
Format:	Artigo
Langue:	Inglês
Publié:	Elsevier 2024-09-01
Collection:	Radiology Case Reports
Sujets:	Alagille syndrome Cholestasis Liver transplantation Ultrasound
Accès en ligne:	http://www.sciencedirect.com/science/article/pii/S1930043324005168
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