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进行性家族性肝内胆汁淤积症概述。

Overview of Progressive Familial Intrahepatic Cholestasis.

机构信息

Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, Mayo Clinic, 200 First Street Southwest, Rochester, MN 55905, USA. Electronic address: https://twitter.com/SaraHassanMD.

Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, Baylor College of Medicine, Texas Children's Hospital, 6621 Fannin Street, Houston, TX 77030, USA.

出版信息

Clin Liver Dis. 2022 Aug;26(3):371-390. doi: 10.1016/j.cld.2022.03.003.

Abstract

Bile acid transport is a complex physiologic process, of which disruption at any step can lead to progressive intrahepatic cholestasis (PFIC). The first described PFIC disorders were originally named as such before identification of a genetic cause. However, advances in clinical molecular genetics have led to the identification of additional disorders that can cause these monogenic inherited cholestasis syndromes, and they are now increasingly referred to by the affected protein causing disease. The list of PFIC disorders is expected to grow as more causative genes are discovered. Here forth, we present a comprehensive overview of known PFIC disorders.

摘要

胆汁酸转运是一个复杂的生理过程,其任何步骤的破坏都可能导致进行性肝内胆汁淤积症(PFIC)。最初描述的 PFIC 疾病在确定遗传原因之前最初就是这样命名的。然而,临床分子遗传学的进步导致了更多可以导致这些单基因遗传性胆汁淤积综合征的疾病的发现,现在它们越来越多地根据引起疾病的相关蛋白来命名。随着更多致病基因的发现,PFIC 疾病的列表预计将会增加。在此,我们全面概述了已知的 PFIC 疾病。

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