Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

J Pediatr. 1991 May;118(5):744-6. doi: 10.1016/s0022-3476(05)80039-3.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • 3-Hydroxyacyl CoA Dehydrogenases / deficiency
  • Biopsy
  • Carnitine / administration & dosage
  • Child
  • Combined Modality Therapy
  • Dietary Fats / administration & dosage
  • Humans
  • Male
  • Mitochondria, Muscle / metabolism
  • Mitochondria, Muscle / ultrastructure
  • Myoglobinuria / diagnosis*
  • Myoglobinuria / metabolism
  • Myoglobinuria / therapy
  • Nervous System Diseases / diagnosis*
  • Nervous System Diseases / metabolism
  • Nervous System Diseases / therapy
  • Neurologic Examination
  • Recurrence
  • Starch / administration & dosage

Substances

  • Dietary Fats
  • Starch
  • 3-Hydroxyacyl CoA Dehydrogenases
  • Carnitine