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Article

Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis associated with Glu89Gln Mutation.

Journal of gastrointestinal and liver diseases : JGLD - 9 Dec 2019

Nakov Radislav, Sarafov Stayko, Nakov Ventsislav, Gospodinova Mariana, Todorov Tihomir, Kirov Andrey, Todorova Albena, Tournev Ivailo

Abstract excerpt

AIMS: In the current study we aimed to explore the prevalence of gastrointestinal (GI) manifestations in hereditary transthyretin amyloid (hATTR) amyloidosis associated with Glu89Gln mutation. METHODS: We recruited 78 patients with hATTR amyloidosis associated with Glu89Gln mutation. The diagnosis of hATTR was defined by a documented transthyretin mutation through DNA analysis. Symptoms were recorded as present...

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Identifiers

PMID: 31826067
DOI: 10.15403/jgld-362

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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