Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation

Eye (Lond). 1995:9 ( Pt 4):513-6. doi: 10.1038/eye.1995.117.

Abstract

Leber's hereditary optic neuropathy (LHON), which is associated with mutations in mitochondrial DNA (mtDNA), is commoner in males than females. A study of over 30 LHON families with a mutation at position 3460 of mtDNA demonstrates a significantly decreased male excess from that generally quoted, with evidence for a marked bias in the ascertainment of males over females. This has implications for the analysis of those factors which give rise to the male bias.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Bias
  • DNA Mutational Analysis
  • DNA, Mitochondrial / genetics*
  • Female
  • Genetic Linkage
  • Humans
  • Male
  • Middle Aged
  • Optic Atrophies, Hereditary / genetics*
  • Pedigree
  • Point Mutation / genetics
  • Sex Factors

Substances

  • DNA, Mitochondrial