Lethal hyperammonaemic coma due to ornithine transcarbamylase deficiency presenting as brain stem encephalitis in a previously asymptomatic ten-year-old boy
- 1 September 1987
- journal article
- case report
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 10 (3) , 271
- https://doi.org/10.1007/bf01800076
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensoriumClinical Genetics, 2008
- Risk of serious illness in heterozygotes for ornithine transcarbamylase deficencyThe Journal of Pediatrics, 1986