Mitochondrial myopathy: a genetic study of 71 cases

J Med Genet. 1988 Aug;25(8):528-35. doi: 10.1136/jmg.25.8.528.

Abstract

Of 71 index cases with histologically defined mitochondrial myopathy, 13 (18%) had relatives who were definitely affected with a similar disorder. Eight familial cases from four families were confined to a single generation. In five families maternal transmission to offspring occurred. There were no instances of paternal transmission, but one patient had an affected cousin in the paternal line. No consistent clinical syndrome or pattern of inheritance emerged for any identified defect of the mitochondrial respiratory chain, localised biochemically in 41 cases. Overall, the recurrence rate was 3% for sibs and 5.5% for offspring of index cases. Review of published reports of familial cases of mitochondrial myopathy suggests that the ratio of maternal to paternal transmission is about 9:1. We conclude that these disorders may be caused by mutations of either nuclear or mitochondrial genes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Central Nervous System Diseases / enzymology
  • Central Nervous System Diseases / epidemiology
  • Central Nervous System Diseases / genetics
  • Female
  • Humans
  • Male
  • Mitochondria, Muscle / enzymology*
  • Muscular Diseases / enzymology
  • Muscular Diseases / epidemiology
  • Muscular Diseases / genetics*
  • Pedigree
  • Succinate Dehydrogenase / genetics

Substances

  • Succinate Dehydrogenase