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Article

Kidney and anemia in familial amyloidosis type I.

Kidney international - 1 Nov 2004

Beirão Idalina, Lobato Luísa, Costa Paulo M P, Fonseca Isabel, Mendes Paula, Silva Manuela, Bravo Fernanda, Cabrita António, Porto Graça

Abstract excerpt

BACKGROUND: Familial amyloid polyneuropathy (FAP) type I is caused by a mutated transthyretin (TTR V30M) and characterized by a sensorimotor and autonomic neuropathy. Renal, cardiac, and ocular abnormalities can also occur. Anemia has been described in previous reports, but its prevalence in Portuguese FAP patients is not precisely known. The aim of this study was to estimate the prevalence of anemia in FAP type...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15496172
DOI: 10.1111/j.1523-1755.2004.00971.x

Genes

FAP
TTR

Variants

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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