Transient Hyperammonemia of the Preterm Infant
- 26 October 1978
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 299 (17) , 920-925
- https://doi.org/10.1056/nejm197810262991704
Abstract
We report on five preterm infants (34 to 36 weeks' gestation) in whom an overwhelming illness developed within the first 48 hours of life. Each had mild respiratory distress that progressed within 48 hours to deep coma requiring ventilatory assistance. Ammonia concentrations in the plasma ranged from 844 to 7640 μg per deciliter. Four received exchange transfusion and peritoneal dialysis; ammonia values returned to the normal range (<150 μg per deciliter) within 72 hours and remained there even after protein challenge. These four subsequently fed and developed normally. The fifth infant died without an attempt to lower plasma ammonia. In this infant (and two of the others) urea-cycle enzymes measured in liver tissue were in the normal range. Transient hyperammonemia of unknown cause may be a relatively common variety of neonatal hyperammonemia; it responds well to prompt diagnosis and aggressive therapy. (N Engl J Med 299:920–925, 1978)This publication has 27 references indexed in Scilit:
- DIABETES MELLITUS AND BONE MINERALPediatric Research, 1977
- Neonatal citrullinemia: Treatment with keto-analogues of essential amino acidsThe Journal of Pediatrics, 1977
- Massive pulmonary hemorrhage as a presenting feature in congenital hyperammonemiaThe Journal of Pediatrics, 1976
- Abnormalities of Carbamyl Phosphate Synthetase and Ornithine Transcarbamylase in Liver of Patients with Reyeʼs SyndromePediatric Research, 1975
- Metabolic and Genetic Studies of a Family with Ornithine Transcarbamylase DeficiencyPediatric Research, 1974
- Ornitbine transcarbamylase deficiency in the newborn infantThe Journal of Pediatrics, 1973
- Carbamylphosphate synthetase deficiency in an infant with severe cerebral damage.Archives of Disease in Childhood, 1969
- Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 PatientsActa Paediatrica, 1967
- Congenital lysine intolerance with periodic ammonia intoxication: A defect in L-lysine degradationMetabolism, 1967
- Argininosuccinic aciduriaThe American Journal of Medicine, 1967