Mitochondrial defects in basal ganglia diseases

Curr Opin Neurol. 1995 Dec;8(6):474-9. doi: 10.1097/00019052-199512000-00015.

Abstract

Mitochondrial DNA mutations are important causes of movement disorders and are often associated with basal ganglia degeneration. Leigh's disease and a form of generalized dystonia are caused by mitochondrial DNA mutations. Recent biochemical and genetic evidence suggests that some cases of Parkinson's disease may be caused by oxidative phosphorylation defects.

Publication types

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

MeSH terms

  • Basal Ganglia Diseases / metabolism*
  • Humans
  • Mitochondria / metabolism*
  • Movement Disorders / metabolism
  • Oxidative Phosphorylation