Results 21 to 30 of about 3,364 (172)

Cholestasis in Benign Recurrent Intrahepatic Cholestasis 2. [PDF]

open access: yesACG Case Rep J, 2020
ABSTRACT Benign recurrent intrahepatic cholestasis represents a rare class of autosomal recessive chronic cholestasis disorders, usually presenting with recurrent episodes of intense pruritus and jaundice. We report a 27-year-old woman presenting with benign recurrent intrahepatic cholestasis type 2 due to heterozygosity in ABCB11 ...
Arthur Lorio E   +3 more
europepmc   +3 more sources

A novel homozygous mutation in the USP53 gene as the cause of benign recurrent intrahepatic cholestasis in children: a case report

open access: yesThe Turkish Journal of Pediatrics, 2023
Background. Benign recurrent intrahepatic cholestasis (BRIC) is a rare cause of cholestasis with recurrent episodes of jaundice and pruritus without extrahepatic bile duct obstruction.
Burcu Berberoğlu Ateş   +5 more
doaj   +3 more sources

Case Report: A Novel Homozygous Variant Identified in a Chinese Patient With Benign Recurrent Intrahepatic Cholestasis-Type 1 [PDF]

open access: yesFrontiers in Medicine, 2021
Benign recurrent intrahepatic cholestasis (BRIC) is a rare hereditary cholestatic liver disorder. Accurate diagnosis and timely interventions are important in determining outcomes.
Huayu Chen   +5 more
doaj   +2 more sources

Benign Recurrent Intrahepatic Cholestasis Type 1 with Novel Nonsense Mutations in the ATP8B1 Gene [PDF]

open access: yesCase Reports in Gastroenterology, 2022
Benign recurrent intrahepatic cholestasis (BRIC) is a group of genetically heterogeneous autosomal recessive liver disorders characterized by recurrent episodes of jaundice and pruritus.
Ryoichi Miura   +20 more
doaj   +2 more sources

The debut of benign recurrent intrahepatic cholestasis in acute hepatitis A

open access: yesТрансплантология (Москва)
Background. Benign recurrent intrahepatic cholestasis is a rare inherited disorder characterized by recurrent episodes of severe hyperbilirubinemia and pruritus that resolve spontaneously.
K. Yu. Kokina   +4 more
doaj   +3 more sources

GGT‐Normal Cholestasis in an Older Child: A Suspected Case of Benign Recurrent Intrahepatic Cholestasis From Syria [PDF]

open access: yesClinical Case Reports
Cholestasis beyond infancy is uncommon and presents a diagnostic challenge. We report an 11‐year‐old girl presenting with severe pruritus followed by jaundice and a cholestatic biochemical profile with normal gamma‐glutamyl transferase levels.
Ahmad Hosiian   +6 more
doaj   +2 more sources

Implantation of nasobiliary drainage in treatment of severe episodes of benign recurrent intrahepatic cholestasis (BRIC) in pediatric patients [PDF]

open access: yesClinical & Experimental Hepatology
Benign recurrent intrahepatic cholestasis (BRIC) is a rare genetic disorder characterized by episodes of intrahepatic cholestasis with varying durations and spontaneous resolutions.
Maciej Dądalski   +7 more
doaj   +2 more sources

BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS (BRIC) [PDF]

open access: yesRomanian Journal of Pediatrics, 2010
Benign recurrent intrahepatic cholestasis (BRIC) a rare form of hereditary cholestasis syndrome characterized by repeated self limited episodes of pruritus and jaundice. It recurs but occasionally leads to progressive liver disease.
S. Arulprakash   +3 more
doaj   +2 more sources

Hyperthyroidism as a Potential Trigger for Benign Recurrent Intrahepatic Cholestasis. [PDF]

open access: yesACG Case Rep J, 2020
ABSTRACT Benign recurrent intrahepatic cholestasis (BRIC) is a rare genetic disease often causing episodes of jaundice since childhood. Its triggering factors are still unknown. Hyperthyroidism solely is an infrequent cause of jaundice, and it was never described in association with BRIC. In this article, we reported a woman presenting with a
Halawi A, Bitar R, Ibrahim N.
europepmc   +3 more sources

Benign Recurrent Intrahepatic Cholestasis: A Case Report

open access: yesSiriraj Medical Journal, 2015
Benign recurrent intrahepatic cholestasis (BRIC) is an autosomal recessive cholestatic liver disease. Recurrent self-limited episodes of jaundice and severe pruritus are leading clinical manifestations.
Prapun Aanpreung, Ananya Pongpaibul
doaj   +4 more sources

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