Late-onset ornithine transcarbamylase deficiency in male patients
Open Access
- 31 December 1990
- journal article
- case report
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 117 (6), 897-902
- https://doi.org/10.1016/s0022-3476(05)80129-5
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensoriumClinical Genetics, 2008
- Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase LocusNew England Journal of Medicine, 1990
- Allopurinol-Induced OrotidinuriaNew England Journal of Medicine, 1990
- Mosaicism for an Intragenic Deletion in a Boy with Mild Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1988
- Ornithine Transcarbamylase Deficiency — A Cause of Bizarre Behavior in a ManNew England Journal of Medicine, 1986
- Risk of serious illness in heterozygotes for ornithine transcarbamylase deficencyThe Journal of Pediatrics, 1986
- Natural History of Symptomatic Partial Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1986
- Chronic benzoate therapy in a boy with partial ornithine transcarbamylase deficiencyThe Journal of Pediatrics, 1985
- Treatment of Inborn Errors of Urea SynthesisNew England Journal of Medicine, 1982
- Ornithine transcarbamylase deficiency in a boy with normal developmentThe Journal of Pediatrics, 1980