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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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| Publicat a: | Proc (Bayl Univ Med Cent) |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Baylor Health Care System
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4462228/ https://ncbi.nlm.nih.gov/pubmed/26130895 |
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