A rare cause of hepatomegaly: 3-hydroxy-3-methylglutaryl coenzyme-a lyase deficiency

J Pediatr Gastroenterol Nutr. 2001 Sep;33(3):339-41. doi: 10.1097/00005176-200109000-00022.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Diagnosis, Differential
  • Female
  • Hepatomegaly / enzymology
  • Hepatomegaly / etiology*
  • Humans
  • Infant
  • Liver / enzymology
  • Liver / pathology
  • Oxo-Acid-Lyases / deficiency*
  • Transaminases / blood

Substances

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