Abstract
Hereditary renal hypouricemia (RHUC) is a rare genetic disorder characterized by a defect of uric acid (UA) reabsorption in the proximal renal tubules, resulting in hypouricemia and increased UA clearance.1 Mutations in the SLC22A12 and SLC2A9 genes, which encode major transporters for UA, have been reported as the cause of RHUC type 1 and type 2, respectively.1
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