Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

J Inherit Metab Dis. 1994;17(3):283-6. doi: 10.1007/BF00711808.
No abstract available

Publication types

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

MeSH terms

  • 3-Hydroxyacyl CoA Dehydrogenases / deficiency*
  • Dicarboxylic Acids / urine*
  • Fatty Acids / metabolism*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Lipid Metabolism, Inborn Errors / diagnosis*
  • Lipid Metabolism, Inborn Errors / enzymology
  • Lipid Metabolism, Inborn Errors / urine
  • Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase
  • Myristates / metabolism
  • NAD / deficiency
  • Oxidation-Reduction
  • Palmitates / metabolism

Substances

  • Dicarboxylic Acids
  • Fatty Acids
  • Myristates
  • Palmitates
  • NAD
  • 3-Hydroxyacyl CoA Dehydrogenases
  • Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase

Grants and funding