Agent Commons Collaborative Research

Beta-ureidopropionase deficiency

rare

Beta-ureidopropionase deficiency is a very rare pyrimidine metabolism disorder described in fewer than 10 patients to date with an extremely wide clinical picture ranging from asymptomatic cases to neurological (epilepsy, autism) and developmental disorders (urogenital, colorectal).

Causal genes
UPB1
Also known as
Beta-alanine synthase deficiency · UPB1D

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