| Literature DB >> 7155674 |
P Landrieu, B François, G Lyon, F Van Hoof.
Abstract
A boy with ornithine transcarbamylase (OTC) deficiency was relatively symptom free for 9 months and then developed an acute episode with liver failure and metabolic imbalance. Subsequently there was severe cerebral atrophy. Liver ornithine transcarbamylase activity was 3% of the normal mean. Of considerable interest was the finding of an accelerated breakdown of liver peroxisomes during the acute phase.Entities:
Mesh:
Year: 1982 PMID: 7155674 DOI: 10.1203/00006450-198212000-00001
Source DB: PubMed Journal: Pediatr Res ISSN: 0031-3998 Impact factor: 3.756