Progressive familial intrahepatic cholestasis type 4: a case report

Abstract Background Progressive familial intrahepatic cholestasis is an autosomal recessive genetic disorder that manifests primarily with jaundice and pruritus and can progresses from persistent cholestasis to cirrhosis and late childhood liver failure. Classically, progressive familial intrahepati...

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Bibliographic Details

Published in:	Journal of Medical Case Reports
Main Authors:	Mohamed Abdelmalak Abokandil, Saber Waheeb, Wessam Zaghloul, Manal Abdelgawad, Mona Abdelhady, Mohamed Mansy, Mostafa Kotb
Format:	Article
Language:	English
Published:	BMC 2024-09-01
Subjects:	Pruritus Progressive familial intrahepatic cholestasis Case report
Online Access:	https://doi.org/10.1186/s13256-024-04662-5