Hyperammonemic coma due to parenteral nutrition in a woman with heterozygous ornithine transcarbamylase deficiency
Open Access
- 1 July 1995
- journal article
- case report
- Published by Elsevier in Gastroenterology
- Vol. 109 (1) , 282-284
- https://doi.org/10.1016/0016-5085(95)90295-3
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Late-onset ornithine transcarbamylase deficiency in male patientsThe Journal of Pediatrics, 1990
- Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase LocusNew England Journal of Medicine, 1990
- Allopurinol-Induced OrotidinuriaNew England Journal of Medicine, 1990
- Prenatal Diagnosis of Ornithine Transcarbamylase Deficiency with Use of DNA PolymorphismsNew England Journal of Medicine, 1986
- Ornithine Transcarbamylase Deficiency — A Cause of Bizarre Behavior in a ManNew England Journal of Medicine, 1986
- Natural History of Symptomatic Partial Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1986
- Risk of serious illness in heterozygotes for ornithine transcarbamylase deficencyThe Journal of Pediatrics, 1986
- Failure of protein loading tests to identify heterozygosity for ornithine carbamoyltransferase deficiencyJournal of Inherited Metabolic Disease, 1984
- Carrier detection in ornithine transcarbamylase deficiencyJournal of Inherited Metabolic Disease, 1980
- Carrier detection in ornithine transcarbamylase deficiencyThe Journal of Pediatrics, 1978