Literature DB >> 21134824

Progressive familial intrahepatic cholestasis.

Tomohide Hori1, Justin H Nguyen, Shinji Uemoto.   

Abstract

BACKGROUND: Three types of progressive familial intrahepatic cholestasis (PFIC) have been identified, but their etiologies include unknown mechanisms. DATA SOURCES: A PubMed search on "progressive familial intrahepatic cholestasis" and "PFIC" was performed on the topic, and the relevant articles were reviewed.
RESULTS: The etiologies of the three PFIC types still include unknown mechanisms. Especially in PFIC type 1, enterohepatic circulation of bile acid should be considered. Ursodeoxycholic acid, partial external biliary diversion and liver transplantation have been used for the treatment of PFIC patients according to disease course.
CONCLUSIONS: Since the etiologies and disease mechanisms of PFIC are still unclear, detailed studies are urgently required. Strategies for more advanced therapies are also needed. These developments in the future are indispensable, especially for PFIC type 1 patients.

Entities:  

Mesh:

Year:  2010        PMID: 21134824

Source DB:  PubMed          Journal:  Hepatobiliary Pancreat Dis Int


  17 in total

Review 1.  Liver transplantation and the management of progressive familial intrahepatic cholestasis in children.

Authors:  Ashley Mehl; Humberto Bohorquez; Maria-Stella Serrano; Gretchen Galliano; Trevor W Reichman
Journal:  World J Transplant       Date:  2016-06-24

2.  Progressive Familial Intrahepatic Cholestasis (PFIC) in Indian Children: Clinical Spectrum and Outcome.

Authors:  Sajan Agarwal; Bikrant Bihari Lal; Dinesh Rawat; Archana Rastogi; Kishore G S Bharathy; Seema Alam
Journal:  J Clin Exp Hepatol       Date:  2016-05-24

Review 3.  Progressive familial intrahepatic cholestasis.

Authors:  Anshu Srivastava
Journal:  J Clin Exp Hepatol       Date:  2013-11-23

4.  Cryptogenic cholestasis in young and adults: ATP8B1, ABCB11, ABCB4, and TJP2 gene variants analysis by high-throughput sequencing.

Authors:  Giovanni Vitale; Stefano Gitto; Francesco Raimondi; Alessandro Mattiaccio; Vilma Mantovani; Ranka Vukotic; Antonietta D'Errico; Marco Seri; Robert B Russell; Pietro Andreone
Journal:  J Gastroenterol       Date:  2017-12-13       Impact factor: 7.527

5.  Novel mutation in a Chinese patient with progressive familial intrahepatic cholestasis type 3.

Authors:  Hao-Zhe Sun; Hong Shi; Shun-Cai Zhang; Xi-Zhong Shen
Journal:  World J Gastroenterol       Date:  2015-01-14       Impact factor: 5.742

6.  miR-33 controls the expression of biliary transporters, and mediates statin- and diet-induced hepatotoxicity.

Authors:  Ryan M Allen; Tyler J Marquart; Carolyn J Albert; Frederick J Suchy; David Q-H Wang; Meenakshisundaram Ananthanarayanan; David A Ford; Angel Baldán
Journal:  EMBO Mol Med       Date:  2012-07-05       Impact factor: 12.137

Review 7.  A Comprehensive Review of Progressive Familial Intrahepatic Cholestasis (PFIC): Genetic Disorders of Hepatocanalicular Transporters.

Authors:  Syed Amer; Amtul Hajira
Journal:  Gastroenterology Res       Date:  2014-05-02

8.  Diagnosis of ABCB11 gene mutations in children with intrahepatic cholestasis using high resolution melting analysis and direct sequencing.

Authors:  Guorui Hu; Ping He; Zhifeng Liu; Qian Chen; Bixia Zheng; Qihua Zhang
Journal:  Mol Med Rep       Date:  2014-06-20       Impact factor: 2.952

9.  Disodium gadoxetate uptake in progressive familial intrahepatic cholestasis type I: Enhancing our understanding of the cholestatic disease.

Authors:  Mikin V Patel; Shlomo Leibowich; Jesse L Courtier; Sue Rhee; John D MacKenzie
Journal:  Radiol Case Rep       Date:  2015-12-07

10.  Bipolar and Related Disorders Induced by Sodium 4-Phenylbutyrate in a Male Adolescent with Bile Salt Export Pump Deficiency Disease.

Authors:  Giovanni Vitale; Giulia Simonetti; Martina Pirillo; Gianfranco Taruschio; Pietro Andreone
Journal:  Psychiatry Investig       Date:  2016-09-30       Impact factor: 2.505

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