6-Methyluracil excretion in 2-methylacetoacetyl-CoA thiolase deficiency and in two children with an unexplained recurrent ketoacidaemia

J Inherit Metab Dis. 1994;17(1):81-4. doi: 10.1007/BF00735400.

Abstract

6-Methyluracil (6MU) has been identified in urine collected during acute illness in two children with beta-ketothiolase deficiency (approximately 1 mmol/L) and in two children with recurrent infection-related ketoacidaemia of unknown aetiology (levels of 6.3 and 7.1 mmol/mmol creatinine). Significant amounts of 6MU were not detected in children with fasting ketosis in whom a metabolic disorder was excluded (normal levels less than 25 mumol/mmol creatinine). We propose that the production of 6MU may be related to the accumulation of acetoacetyl-CoA and thus be a marker for disorders where this occurs.

Publication types

  • Case Reports

MeSH terms

  • Acetyl-CoA C-Acetyltransferase / deficiency*
  • Acetyl-CoA C-Acyltransferase / deficiency
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Keto Acids / blood*
  • Ketosis / blood
  • Ketosis / urine*
  • Male
  • Mass Spectrometry
  • Recurrence
  • Uracil / analogs & derivatives*
  • Uracil / urine

Substances

  • Keto Acids
  • Uracil
  • 6-methyluracil
  • Acetyl-CoA C-Acyltransferase
  • Acetyl-CoA C-Acetyltransferase