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Sickle cell anemia (SCA) is one of the commonest severe inherited disorders affecting millions worldwide. Complications are extensive although severity varies markedly. Renal damage [or sickle cell nephropathy (SCN)] occurs in approximately one-third of SCA children[1][1],[2][2] and a significant

Nocturnal enuresis and K+ transport in red blood cells from patients with sickle cell anemia