Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency

J Med Genet. 2005 May;42(5):e28. doi: 10.1136/jmg.2004.029926.

Abstract

Background: Isolated cytochrome c oxidase (COX) deficiency is usually associated with mutations in several factors involved in the biogenesis of COX.

Methods: We describe a patient with atypical, long surviving Leigh syndrome carrying two novel mutations in the COX15 gene, which encodes an enzyme involved in the biosynthesis of heme A.

Results: Only two COX15 mutated patients, one with severe neonatal cardiomyopathy, the other with rapidly fatal Leigh syndrome, have been described to date. In contrast, our patient had a slowly progressive course with no heart involvement. COX deficiency was mild in muscle and a normal amount of fully assembled COX was present in cultured fibroblasts.

Conclusions: The clinical and biochemical phenotypes in COX15 defects are more heterogeneous than in other conditions associated with COX deficiency, such as mutations in SURF1.

Publication types

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

MeSH terms

  • Adolescent
  • Brain / pathology
  • Cytochrome-c Oxidase Deficiency / genetics*
  • Cytochrome-c Oxidase Deficiency / pathology
  • DNA Mutational Analysis
  • Electron Transport Complex IV / genetics*
  • Electron Transport Complex IV / metabolism
  • Fibroblasts / pathology
  • Humans
  • Leigh Disease / genetics*
  • Leigh Disease / pathology
  • Male
  • Mutation*
  • Survivors

Substances

  • Electron Transport Complex IV