Recurrent myoglobinuria as a presenting manifestation of very long chain acyl coenzyme A dehydrogenase deficiency

Pediatrics. 1997 Jun;99(6):894-6. doi: 10.1542/peds.99.6.894.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Acyl-CoA Dehydrogenase, Long-Chain
  • Age of Onset
  • Carnitine
  • Child
  • Diet
  • Fatty Acid Desaturases / deficiency*
  • Female
  • Food, Fortified
  • Humans
  • Metabolism, Inborn Errors / complications
  • Metabolism, Inborn Errors / diagnosis*
  • Metabolism, Inborn Errors / therapy
  • Myoglobinuria / etiology*
  • Myoglobinuria / therapy
  • Recurrence

Substances

  • Fatty Acid Desaturases
  • Acyl-CoA Dehydrogenase, Long-Chain
  • Carnitine