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Indian J Pediatr ; 1997 Mar-Apr; 64(2): 266-9
Article in English | IMSEAR | ID: sea-83492

ABSTRACT

Hyperargininemia due to arginase deficiency is a rare, inherited, urea cycle disorder. We report a case of arginase deficiency in a 5-year old boy presenting with mild hyperammonemia, hyperargininemia, and dibasic aminoaciduria.


Subject(s)
Arginase/deficiency , Child, Preschool , Chromosome Aberrations/genetics , Chromosome Disorders , Genes, Recessive , Humans , Hyperargininemia/diagnosis , Male
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