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Clinical features of carbamyl phosphate synthetase‐I deficiency in an adult
Author(s) -
Call Gregory,
Seay Alan R.,
Sherry Richard,
Qureshi Ijaz A.
Publication year - 1984
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.410160118
Subject(s) - hyperammonemia , urea cycle , carbamyl phosphate , encephalopathy , lactulose , pediatrics , medicine , leukodystrophy , white matter , metabolic disorder , gastroenterology , endocrinology , cardiology , disease , magnetic resonance imaging , chemistry , biochemistry , radiology , amino acid , arginine , enzyme
Carbamyl phosphate synthetase‐I (CPS‐I) catalyzes the first reaction required for the conversion of ammonia to urea through the urea cycle. Severe CPS‐I deficiency causes marked hyperammonemia with encephalopathy in infancy and usually results in death within the first few months of life. We describe a 33‐year‐old woman whose CPS‐I activity is less than 5% of normal. She has had mild, intermittent symptoms throughout life but has never experienced severe encephalopathy. Although mildly retarded, she has no major neurological deficits. Therapy with a low‐protein diet, lactulose, and sodium benzoate has prevented recurrence of hyperammonemia and symptoms. Cranial computed tomographic scans demonstrate prominent lucency of cerebral white matter, and cerebral evoked potential recordings indicate slowed central conduction. These findings suggest that the metabolic disturbances in this patient may have adversely affected central myelin formation or maintenance. This woman represents, to our knowledge, the oldest reported patient with CPS‐I deficiency, and the case illustrates the need to consider urea cycle disorders in the differential diagnosis of intermittent neurological symptoms regardless of the patient's age.