Mitochondrial very long-chain acyl-CoA dehydrogenase deficiency with a mild clinical course

J Inherit Metab Dis. 1996;19(2):173-6. doi: 10.1007/BF01799422.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acidosis / etiology
  • Acyl-CoA Dehydrogenase, Long-Chain / deficiency*
  • Carboxylic Acids / blood
  • Carboxylic Acids / urine
  • Cardiomyopathies / etiology
  • Child
  • Female
  • Humans
  • Hypoglycemia / etiology
  • Liver Diseases / etiology
  • Mitochondria / enzymology*

Substances

  • Carboxylic Acids
  • Acyl-CoA Dehydrogenase, Long-Chain