Neonatal hyperammonemia: the N-carbamoyl-L-glutamic acid test

J Pediatr. 2005 Aug;147(2):260-2. doi: 10.1016/j.jpeds.2005.04.059.

Abstract

In a prospective study, patients with a suspected urea cycle defect underwent oral N-carbamoyl-L-glutamic acid loading testing. In patients with subsequently confirmed N-acetylglutamate synthase deficiency, hyperammonemia normalized within 8 hours. This test may be useful in the early diagnosis of patients with suspected urea cycle disorders.

Publication types

  • Case Reports

MeSH terms

  • Acetyltransferases / deficiency*
  • Amino-Acid N-Acetyltransferase
  • Fatal Outcome
  • Female
  • Glutamates / therapeutic use*
  • Humans
  • Hyperammonemia / diagnosis
  • Hyperammonemia / drug therapy*
  • Infant
  • Infant, Newborn
  • Male

Substances

  • Glutamates
  • N-carbamylglutamate
  • Acetyltransferases
  • Amino-Acid N-Acetyltransferase
  • NAGS protein, human