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Autor:
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
Publikováno v:
Radiology Case Reports, Vol 19, Iss 9, Pp 4082-4086 (2024)
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 di
Externí odkaz:
https://doaj.org/article/fdced301cf8045e393797a2f398687fb
