نتایج جستجو برای: ornithine transcarbamylase

تعداد نتایج: 5759  

2008
Jacob F Collen Nealanjon P Das Jonathan M Koff Robert T Neff Kevin C Abbott

Acute hyperammonemia is a medical emergency requiring rapid recognition and treatment to prevent devastating neurologic sequelae. Its varying etiologies include primary hepatic failure, drug toxicity, infection, and inherited disorders of metabolism. Ornithine transcarbamylase (OTC) deficiency is the most common inherited urea cycle disorder and can result in hyperammonemic encephalopathy and c...

Journal: :Journal of pediatric surgery 1995
T Hasegawa A G Tzakis S Todo J Reyes B Nour D N Finegold T E Starzl

Ornithine transcarbamylase (OTC) deficiency is an X chromosome-linked disorder causing hyperammonemic encephalopathy with a very poor prognosis. We describe here two patients with OTC deficiency, one a late on-set female patient (case 1) and the other a neonatal-onset male patient (case 2), who were successfully treated with orthotopic liver transplantation (OLTx). The OTC activity in the excis...

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