Lethal dilated cardiomyopathy due to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

J Inherit Metab Dis. 1996;19(3):373-4. doi: 10.1007/BF01799273.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • 3-Hydroxyacyl CoA Dehydrogenases / deficiency*
  • Cardiomyopathy, Dilated / etiology*
  • Humans
  • Infant
  • Male

Substances

  • 3-Hydroxyacyl CoA Dehydrogenases