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Article

Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients.

La Tunisie medicale - 1 Apr 2015

Chaouch Leila, Kalai Miniar, Chaouachi Dorra, Mallouli Fethi, Hafsia Raouf, Ben Ammar Slim, Abbes Salem

Abstract excerpt

BACKGROUND: As a result of chronic hemolysis, hyperbilirubinemia is often observed, leading to the formation of pigment cholelithiasis which could be busted by the presence of uridine diphosphoglucuronosyltransferase 1A1 defects. AIM: Herein, we investigated the effect of glibert mutation on the occurrence of pigment cholelithiasis in Tunisian patients with beta (β) hemoglobinopathy including sickle cell anemia...

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PMID: 26375741

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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