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Article

[Wolfram syndrome: from definition to molecular bases].

Arquivos brasileiros de endocrinologia e metabologia - 1 Oct 2006

Ribeiro Maria Regina F, Crispim Felipe, Vendramini Márcio F, Moisés Regina S

Abstract excerpt

Wolfram syndrome (WS) is an autosomal recessive progressive neurodegenerative disorder characterized by diabetes mellitus and optic atrophy. Diabetes insipidus and sensorineural deafness are also noted frequently, explaining the acronym DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy and deafness) by which the syndrome is also referred. Additional manifestations such as atonic bladder, ataxia,...

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Identifiers

PMID: 17160206
DOI: 10.1590/s0004-27302006000500003

Genes

WFS1

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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