A case of Ohtahara syndrome with cytochrome oxidase deficiency

Dev Med Child Neurol. 1998 Aug;40(8):568-70. doi: 10.1111/j.1469-8749.1998.tb15416.x.

Abstract

Ohtahara syndrome is a rare cause of epileptic seizures during the neonatal period. This is believed to be the first report of this syndrome with a specific metabolic defect. Defects in respiratory chain function may be more common than previously assumed in patients with this epilepsy syndrome.

Publication types

  • Case Reports

MeSH terms

  • Cytochrome-c Oxidase Deficiency*
  • Electroencephalography
  • Electron Transport / physiology
  • Electron Transport Complex IV / metabolism*
  • Epilepsy / diagnosis
  • Epilepsy / enzymology*
  • Humans
  • Infant, Newborn
  • Male
  • Syndrome

Substances

  • Electron Transport Complex IV