Detection of urinary hexanoylglycine in the diagnosis of MCAD deficiency from newborn screening

J Inherit Metab Dis. 2008 Aug;31(4):550. doi: 10.1007/s10545-008-9976-z.
No abstract available

Publication types

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

MeSH terms

  • Acyl-CoA Dehydrogenase / deficiency*
  • Clinical Laboratory Techniques
  • Glycine / analogs & derivatives*
  • Glycine / analysis
  • Glycine / urine
  • Humans
  • Infant, Newborn
  • Metabolic Diseases / diagnosis*
  • Multicenter Studies as Topic
  • Neonatal Screening / methods*
  • Pilot Projects
  • Sensitivity and Specificity
  • United Kingdom

Substances

  • N-caproylglycine
  • Acyl-CoA Dehydrogenase
  • Glycine