Diagnosis and treatment in a case of juvenile subacute necrotizing encephalopathy Leigh without cytochrome c oxidase deficiency

Eur Neurol. 1992;32(4):206-11. doi: 10.1159/000116823.

Abstract

Subacute necrotizing encephalopathy (Leigh syndrome) is characterized by lactacidosis, seizures, ataxia, multiple cerebral hypervascularized lesions and mitochondrial oxidation defects. This is a report on a 21-year-old patient with proven Leigh syndrome, mild central and provokable peripheral lactacidosis, an extra-erythrocyte complex II defect, functionally reduced myokinase adenylate deaminase activity, but no ultrastructural mitochondrial changes. Determination of lactate, pyruvate and ammonia under ischemic conditions plus a pyruvate loading test were particularly useful. Oral flunarizine (Sibelium 30 mg/d) proved to be therapeutically effective.

Publication types

  • Case Reports

MeSH terms

  • Biopsy
  • Cytochrome-c Oxidase Deficiency*
  • Electron Transport Complex IV / physiology
  • Female
  • Flunarizine / therapeutic use
  • Humans
  • Leigh Disease / diagnosis*
  • Leigh Disease / drug therapy
  • Leigh Disease / physiopathology
  • Magnetic Resonance Imaging
  • Motor Cortex / pathology
  • Muscles / pathology
  • Neurologic Examination / drug effects
  • Neurons / pathology
  • Neuropsychological Tests
  • Tomography, X-Ray Computed

Substances

  • Electron Transport Complex IV
  • Flunarizine