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Related to renal glucosuria: endoplasmic reticulum, Fanconi syndrome, Primary renal glycosuria
renal glucosuriaAn autosomal recessive disorder (OMIM:233100) characterised by a normal fasting serum glucose levels and persistent isolated glucosuria, with a normal glucose tolerance test.
Defects of SLC5A2, which encodes a sodium-dependent glucose cotransporter involved in glucose reabsorption in the proximal tubules, cause renal glucosuria.
1. the presence of glucose in the urine.
2. dextrosuria. Called also glycosuria.
glucosuria due to an inherited inability of renal tubules to reabsorb glucose completely.