Arginase deficiency

Arginase deficiency is a rare autosomal recessive amino acid metabolism disorder characterized clinically by variable degrees of hyperammonemia, developing from about 3 years of age, and leading to progressive loss of developmental milestones and spasticity in the absence of treatment.

Also known as: arginase deficiency, argininemia, hyperargininemia, Arg1 deficiency

11 clinical trials for this condition and its sub-types, 8 tagged with Arginase deficiency itself.