Progressive depletion of mtDNA in mitochondrial myopathy.

Durham, Steve E; Brown, Denise T; Turnbull, Douglass M; Chinnery, Patrick F · Neurology · 2006

case_series · Level IV

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Abstract

The authors studied seven patients with mitochondrial DNA (mtDNA) myopathy. Over time, there was a progressive depletion of mtDNA, which preferentially affected wild-type mitochondrial genomes. This suggests that loss of wild-type mtDNA is a major feature of mtDNA myopathy, and preventing wild-type mtDNA depletion has treatment implications.

Medical subject headings