Carbamoyl-Phosphate Synthase I Deficiency Disease D020165

Related MeSH Hierarchy (7)

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Mitochondrial Diseases » Carbamoyl-Phosphate Synthase I Deficiency Disease

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Brain Diseases, Metabolic » Brain Diseases, Metabolic, Inborn » Urea Cycle Disorders, Inborn » Carbamoyl-Phosphate Synthase I Deficiency Disease

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Brain Diseases, Metabolic, Inborn » Urea Cycle Disorders, Inborn » Carbamoyl-Phosphate Synthase I Deficiency Disease

Description

A urea cycle disorder manifesting in infancy as lethargy, emesis, seizures, alterations of muscle tone, abnormal eye movements, and an elevation of serum ammonia. The disorder is caused by a reduction in the activity of hepatic mitochondrial CARBAMOYL-PHOSPHATE SYNTHASE (AMMONIA). (Menkes, Textbook of Child Neurology, 5th ed, pp50-1)   MeSH

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