the urea cycle, results in hyperammonemia. The X-linked recessive inheritance results in neonatal death of affected males but a variable symptomatic pattern in females, with onset of symptoms in childhood. We report the cases of two heterozygous women with onset of severe symptoms (encephalopathy and focal neurologic deficits) in adulthood
Abstract X-linked ornithine transcarbamylase deficiency (OTCD) is the most common urea cycle disorde...
X-linked ornithine transcarbamylase deficiency (OTCD) is the most common urea cycle disorder. Hemizy...
Abstract Hyperammonemia is one of the common complications of porto-systemic shunt or liver failure....
Urea cycle enzymes deficiencies are rare metabolic disorders. Ornithine transcarbamylase (OTC) defic...
Ornithine transcarbamylase (OTC) deficiency is an X-linked urea cycle defect. While hemizygous males...
Urea cycle disorders (UCDs) are a group of rare inherited metabolic conditions caused by enzyme defi...
Objectives To report the clinical manifestations of acute hyperammonemic encephalopathy in adult ons...
Ornithine transcarbamylase deficiency (OTCD) is a rare X-linked disorder of urea synthesis leading t...
Ornithine transcarbamylase deficiency (OTCD) is a rare X-linked disorder of urea synthesis leading t...
Introduction: Ornithine transcarbamylase deficiency is the most common inherited disorder of the ure...
Copyright © 2015 Jordi Gascon-Bayarri et al. This is an open access article distributed under the Cr...
Background & AimsLate-onset symptoms of urea-cycle disorder may lead to a life-threatening disease w...
We report on a family with ornithine transcarbamylase (OTC) deficiency, an X-linked urea cycle disor...
Ornithine transcarbamylase deficiency (OMIM: 311250) is the most common disorder of urea cycle disor...
Late-onset symptoms of urea-cycle disorder may lead to a life-threatening disease which is often und...
Abstract X-linked ornithine transcarbamylase deficiency (OTCD) is the most common urea cycle disorde...
X-linked ornithine transcarbamylase deficiency (OTCD) is the most common urea cycle disorder. Hemizy...
Abstract Hyperammonemia is one of the common complications of porto-systemic shunt or liver failure....
Urea cycle enzymes deficiencies are rare metabolic disorders. Ornithine transcarbamylase (OTC) defic...
Ornithine transcarbamylase (OTC) deficiency is an X-linked urea cycle defect. While hemizygous males...
Urea cycle disorders (UCDs) are a group of rare inherited metabolic conditions caused by enzyme defi...
Objectives To report the clinical manifestations of acute hyperammonemic encephalopathy in adult ons...
Ornithine transcarbamylase deficiency (OTCD) is a rare X-linked disorder of urea synthesis leading t...
Ornithine transcarbamylase deficiency (OTCD) is a rare X-linked disorder of urea synthesis leading t...
Introduction: Ornithine transcarbamylase deficiency is the most common inherited disorder of the ure...
Copyright © 2015 Jordi Gascon-Bayarri et al. This is an open access article distributed under the Cr...
Background & AimsLate-onset symptoms of urea-cycle disorder may lead to a life-threatening disease w...
We report on a family with ornithine transcarbamylase (OTC) deficiency, an X-linked urea cycle disor...
Ornithine transcarbamylase deficiency (OMIM: 311250) is the most common disorder of urea cycle disor...
Late-onset symptoms of urea-cycle disorder may lead to a life-threatening disease which is often und...
Abstract X-linked ornithine transcarbamylase deficiency (OTCD) is the most common urea cycle disorde...
X-linked ornithine transcarbamylase deficiency (OTCD) is the most common urea cycle disorder. Hemizy...
Abstract Hyperammonemia is one of the common complications of porto-systemic shunt or liver failure....