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Nonhepatic hyperammonemic encephalopathy due to undiagnosed urea cycle disorder

Ornithine transcarbamoylase deficiency is the most common inherited urea cycle disorder. In adults, its phenotypes are diverse. In asymptomatic patients with late presentations, symptom onset is often associated with a precipitating factor. We present a case of a woman with urea cycle disorder diagn...

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Bibliographic Details
Published in:Proc (Bayl Univ Med Cent)
Main Authors: Mahmood, Tashfeen, Nugent, Kenneth
Format: Artigo
Language:Inglês
Published: Baylor Health Care System 2015
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4462228/
https://ncbi.nlm.nih.gov/pubmed/26130895
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