3-Hydroxy-3-methylglutaryl-CoA lyase deficiency: absence of clinical symptoms due to a self-imposed dietary fat and protein restriction

J Inherit Metab Dis. 1993;16(6):1061-2. doi: 10.1007/BF00711535.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / diagnosis
  • Amino Acid Metabolism, Inborn Errors / diet therapy*
  • Amino Acid Metabolism, Inborn Errors / enzymology*
  • Child
  • Dietary Fats / administration & dosage*
  • Dietary Proteins / administration & dosage*
  • Female
  • Humans
  • Oxo-Acid-Lyases / deficiency*

Substances

  • Dietary Fats
  • Dietary Proteins
  • Oxo-Acid-Lyases
  • 3-hydroxy-3-methylglutaryl-coenzyme A lyase