| Literature DB >> 16227111 |
Marshall L Summar1, Frederick Barr, Sheila Dawling, Wendy Smith, Brendan Lee, Rani H Singh, William J Rhead, Lisa Sniderman King, Brian W Christman.
Abstract
Most often, urea cycle disorders have been described as acute onset hyperammonemia in the newborn period; however, there is a growing awareness that urea cycle disorders can present at almost any age, frequently in the critical care setting. This article presents three cases of adult-onset hyperammonemia caused by inherited defects in nitrogen processing in the urea cycle, and reviews the diagnosis, management, and pathophysiology of adult-onset urea cycle disorders. Individuals who have milder molecular urea cycle defects can lead a relatively normal life until a severe environmental stress triggers a hyperammonemic crisis. Comorbid conditions such as physical trauma often delay the diagnosis of the urea cycle defect. Prompt recognition and treatment are essential in determining the outcome of these patients.Entities:
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Year: 2005 PMID: 16227111 DOI: 10.1016/j.ccc.2005.05.002
Source DB: PubMed Journal: Crit Care Clin ISSN: 0749-0704 Impact factor: 3.598