Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: different clinical expression in three unrelated patients

J Inherit Metab Dis. 1991;14(3):325-8. doi: 10.1007/BF01811694.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • 3-Hydroxyacyl CoA Dehydrogenases / deficiency*
  • Child
  • Child, Preschool
  • Female
  • Fibroblasts / enzymology
  • Humans
  • Hypoglycemia / blood
  • Hypoglycemia / etiology
  • Infant
  • Infant, Newborn
  • Infant, Premature
  • Lipid Metabolism, Inborn Errors / diet therapy
  • Lipid Metabolism, Inborn Errors / enzymology*
  • Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase
  • Mitochondria, Liver / enzymology

Substances

  • 3-Hydroxyacyl CoA Dehydrogenases
  • Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase