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[Diabetes and hearing impairment due to mitochondrial mutation].

Ugeskrift for laeger - 15 Sept 2014

Lauterlein Jens-Jacob, Olsen Inger, Yderstræde Knud, Nielsen Morten Frost

Abstract excerpt

Mutations in the mitochondrial genome can cause mitochondrial diabetes. We present two cases in which the same mutation, mtDNA3243A>G, caused two different phenotypes: maternally inherited diabetes and deafness and mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes. Mitochondrial disease can imitate a variety of common con-ditions and should be considered in the case of multisystem...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 25294200

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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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