Ontology highlight
ABSTRACT:
SUBMITTER: Kido J
PROVIDER: S-EPMC5332424 | biostudies-literature | 2017 Feb
REPOSITORIES: biostudies-literature
Kido Jun J Kawasaki Tatsuya T Mitsubuchi Hiroshi H Kamohara Hidenobu H Ohba Takashi T Matsumoto Shirou S Endo Fumio F Nakamura Kimitoshi K
World journal of hepatology 20170201 6
Ornithine transcarbamylase deficiency (OTCD) is an X-linked disorder, with an estimated prevalence of 1 per 80000 live births. Female patients with OTCD develop metabolic crises that are easily provoked by non-predictable common disorders, such as genetic (private mutations and lyonization) and external factors; however, the outcomes of these conditions may differ. We resuscitated a female patient with OTCD from hyperammonemic crisis after she gave birth. Hyperammonemia after parturition in a fe ...[more]