[Specific enzyme diagnosis in mitochondrial myopathies and encephalomyopathies]

Orv Hetil. 1994 Apr 3;135(14):747-50.
[Article in Hungarian]

Abstract

Mitochondrial enzyme activities (cytochrome c-oxidase = COX, carnitine acyl-transferase = CAT, citrate synthase = CS, lipoamide dehydrogenase = lipDH from the pyruvate-dehydrogenase complex, lactate dehydrogenase = LDH, and malate-dehydrogenase = MDH) were measured from progressive myopathy/encephalomyopathy. Cytochrome oxidase (COX) deficiency was detected from muscle or liver tissues, adult type of COX defectus had been diagnosed in 1 case and infantile type in further 6 cases. The 3 familial atactic children showed decreased activity of carnitine acetyl-transferase, too.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Clinical Enzyme Tests*
  • Electron Transport Complex IV / blood
  • Humans
  • Infant
  • L-Lactate Dehydrogenase / blood
  • Liver / enzymology
  • Male
  • Mitochondrial Encephalomyopathies / diagnosis
  • Mitochondrial Encephalomyopathies / enzymology*
  • Mitochondrial Myopathies / diagnosis
  • Mitochondrial Myopathies / enzymology*
  • Muscles / enzymology
  • Pyruvate Dehydrogenase Complex / blood

Substances

  • Pyruvate Dehydrogenase Complex
  • L-Lactate Dehydrogenase
  • Electron Transport Complex IV