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Article

THAOS: gastrointestinal manifestations of transthyretin amyloidosis - common complications of a rare disease.

Orphanet journal of rare diseases - 27 Apr 2014

Wixner Jonas, Mundayat Rajiv, Karayal Onur N, Anan Intissar, Karling Pontus, Suhr Ole B

Abstract excerpt

BACKGROUND: Transthyretin amyloidosis is a systemic disorder caused by amyloid deposits formed by misfolded transthyretin monomers. Two main forms exist: hereditary and wild-type transthyretin amyloidosis, the former associated with transthyretin gene mutations. There are several disease manifestations; however, gastrointestinal complications are common in the hereditary form. The aim of this study was to explore...

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Source

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Identifiers

PMID: 24767411
DOI: 10.1186/1750-1172-9-61
PMCID: PMC4005902

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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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