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Article

Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G.

Acta medica portuguesa - 31 Aug 2017

Alves Daniela, Calmeiro Maria Eufémia, Macário Carmo, Silva Rosa

Abstract excerpt

Maternally inherited diabetes and deafness is a rare form of diabetes caused by a mitochondrial DNA mutation. The index case is a 55-year-old woman who was admitted with hypertrophic cardiomyopathy. She had a history of diabetes mellitus and hearing loss. The patient's mother, two brothers and two sisters also had a history of diabetes and hearing loss. This pattern suggests a maternally inherited disorder. All...

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Source

Identifiers

PMID: 28926334
DOI: 10.20344/amp.8638

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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