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Article

Evaluation of previously nonscreened hereditary hemorrhagic telangiectasia patients shows frequent liver involvement and early cardiac consequences.

Hepatology (Baltimore, Md.) - 1 Nov 2008

Gincul Rodica, Lesca Gaetan, Gelas-Dore Bénédicte, Rollin Nathalie, Barthelet Martine, Dupuis-Girod Sophie, Pilleul Franck, Giraud Sophie, Plauchu Henri, Saurin Jean-Christophe

Abstract excerpt

UNLABELLED: Hereditary hemorrhagic telangiectasia (HHT) is a genetic disease characterized by cutaneous, mucosal, and sometimes visceral arteriovenous malformations. Severe hepatic manifestations have been characterized in a subgroup of patients, but few data are available in previously nonscreened patients. We prospectively evaluated liver involvement and its cardiac consequences in such patients. Between 2000...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18972447
DOI: 10.1002/hep.22514

Genes

ACVRL1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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