» Articles » PMID: 6618106

Familial Occurrence of Primary Sclerosing Cholangitis and Ulcerative Colitis

Overview
Specialty Gastroenterology
Date 1983 Nov 1
PMID 6618106
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Members of three families had primary sclerosing cholangitis and chronic ulcerative colitis. In each family, two siblings were affected; in one instance, they were twin brothers. All six individuals had primary sclerosing cholangitis and five also had ulcerative colitis. These cases represent the first reported instances of the familial occurrence of both primary sclerosing cholangitis and chronic ulcerative colitis; illustrate the typical clinical, laboratory, radiologic, and pathological features of primary sclerosing cholangitis; and support the hypothesis that genetic factors may play a role in the etiology of this obscure disorder.

Citing Articles

Targeting the Gut Microbiome as a Treatment for Primary Sclerosing Cholangitis: A Conceptional Framework.

Shah A, Macdonald G, Morrison M, Holtmann G Am J Gastroenterol. 2020; 115(6):814-822.

PMID: 32250997 PMC: 7269024. DOI: 10.14309/ajg.0000000000000604.


Primary sclerosing cholangitis: A review and update.

Tabibian J, Bowlus C Liver Res. 2018; 1(4):221-230.

PMID: 29977644 PMC: 6028044. DOI: 10.1016/j.livres.2017.12.002.


Hepatobiliary Manifestations and Complications in Inflammatory Bowel Disease: A Review.

Fousekis F, Theopistos V, Katsanos K, Tsianos E, Christodoulou D Gastroenterology Res. 2018; 11(2):83-94.

PMID: 29707074 PMC: 5916631. DOI: 10.14740/gr990w.


Recurrence of autoimmune liver diseases after liver transplantation.

Faisal N, Renner E World J Hepatol. 2015; 7(29):2896-905.

PMID: 26689244 PMC: 4678376. DOI: 10.4254/wjh.v7.i29.2896.


Patients, cells, and organelles: the intersection of science and serendipity.

LaRusso N Hepatology. 2011; 53(5):1417-26.

PMID: 21413050 PMC: 3082583. DOI: 10.1002/hep.24297.