Aminoaciduria and Glycosuria in Children

Abstract

Only negligible amounts of amino acids and glucose are normally present in the final urine, reflecting very efficient reabsorption mechanisms for these organic solutes in the proximal tubule. Renal tubular transport defects or specific metabolic abnormalities result in excretion of significant quantities of amino acids or glucose in the urine. Although hereditary defects in renal tubular transport of most of these substances are uncommon, they are of major biologic importance. First, some of these membrane transport disorders (e.g., cystinuria, lysinuric protein intolerance, Hartnup disease) are associated with significant morbidity. Second, the study of these disorders has provided much insight into the physiology of renal tubular reclamation of amino acids and glucose and into the specific metabolic pathways that control their reabsorption and has been crucial in understanding the genetics of tubular transport systems.