Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

J Inherit Metab Dis. 1990;13(5):752-3. doi: 10.1007/BF01799579.
No abstract available

Publication types

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

MeSH terms

  • Death, Sudden / etiology*
  • Food, Formulated
  • Humans
  • Infant
  • Male
  • Oxo-Acid-Lyases / deficiency*

Substances

  • Oxo-Acid-Lyases
  • 3-hydroxy-3-methylglutaryl-coenzyme A lyase