Episodic ataxia and hemiplegia caused by the 8993T->C mitochondrial DNA mutation

J Med Genet. 2007 Dec;44(12):797-9. doi: 10.1136/jmg.2007.052902.

Abstract

The m.8993T-->C MTATP6 mutation of mitochondrial DNA (mtDNA) usually causes mitochondrial disease in childhood, but was recently described in a family with adult onset ataxia and polyneuropathy. Cytochrome c oxidase muscle histochemistry, which is the standard clinical investigation for mitochondrial disease in adults, is usually normal in patients with MTATP6 mutations. This raises the possibility that these cases have been missed in the past. We therefore studied 308 patients with unexplained ataxia and 96 patients with suspected Charcot-Marie-Tooth disease to determine whether the m.8993T-->C MTATP6 mutation is common in unexplained inherited ataxia and/or polyneuropathy. We identified a three-generation family with the m.8993T-->C mutation of mtDNA. One subject had episodic ataxia (EA) and transient hemipareses, broadening the phenotype. However, no further cases were identified in an additional cohort of 191 patients with suspected EA. In conclusion, m.8993T-->C MTATP6 should be considered in patients with unexplained ataxia, CMT or EA, but cases are uncommon.

Publication types

  • Case Reports
  • Comparative Study
  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Aged
  • Charcot-Marie-Tooth Disease / genetics
  • Cohort Studies
  • DNA, Mitochondrial / genetics
  • Dysarthria / genetics
  • Female
  • Genetic Heterogeneity
  • Hereditary Sensory and Motor Neuropathy / diagnosis
  • Hereditary Sensory and Motor Neuropathy / genetics*
  • Humans
  • Middle Aged
  • Mitochondrial Diseases / genetics*
  • Mitochondrial Proton-Translocating ATPases / deficiency
  • Mitochondrial Proton-Translocating ATPases / genetics*
  • Mutation, Missense*
  • Ocular Motility Disorders / genetics
  • Paresis / genetics*
  • Pedigree
  • Periodicity
  • Point Mutation*
  • Spinocerebellar Degenerations / genetics*

Substances

  • DNA, Mitochondrial
  • MT-ATP6 protein, human
  • Mitochondrial Proton-Translocating ATPases