[Neonatal hyperammonemia]

Tijdschr Kindergeneeskd. 1983 Jun;51(3):101-4.
[Article in Dutch]

Abstract

Experience with severe neonatal hyperammonaemia in the Newborn Intensive Care Unit of the Leuven University Hospital is reported and compared with the literature data. Among eleven patients seven presented with the transient neonatal hyperammonaemia-syndrome and four with a urea cycle defect. Prompt recognition of the transient neonatal hyperammonaemia syndrome is important because its prognosis is much better than that of the primary urea cycle defects presenting in the neonatal period.

Publication types

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

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / blood*
  • Ammonia / blood*
  • Argininosuccinic Aciduria
  • Carbamoyl-Phosphate Synthase (Ammonia) / deficiency
  • Diagnosis, Differential
  • Humans
  • Infant, Newborn
  • Infant, Premature, Diseases / blood*
  • Metabolism, Inborn Errors / blood*
  • Ornithine Carbamoyltransferase Deficiency Disease
  • Urea / blood

Substances

  • Ammonia
  • Urea
  • Carbamoyl-Phosphate Synthase (Ammonia)