Duplications of mitochondrial DNA in Kearns-Sayre syndrome

Muscle Nerve Suppl. 1995:3:S154-8. doi: 10.1002/mus.880181430.

Abstract

mtDNA duplications were detectable in 10 of 10 patients with mtDNA deletions and Kearns-Sayre syndrome (KSS) and in none of 8 patients with chronic progressive external ophthalmoplegia (CPEO). Thus, duplications of mtDNA seem to be a distinctive feature of KSS, including patients where Pearson's syndrome is the first manifestation. Diabetes mellitus was identified in 4 of 7 patients with high or moderate levels of mtDNA duplications. The balance of mtDNA rearrangements may be central to the pathogenesis of this unique group of disorders.

Publication types

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

MeSH terms

  • Adult
  • Chromosome Deletion*
  • DNA, Mitochondrial / genetics*
  • Diabetes Mellitus / genetics
  • Gene Rearrangement
  • Humans
  • Kearns-Sayre Syndrome / genetics*
  • Ophthalmoplegia / genetics*

Substances

  • DNA, Mitochondrial