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Renal glucosuria

Orpha number ORPHA69076
Prevalence of rare diseases Unknown
Inheritance
  • Autosomal recessive
Age of onset Variable
ICD 10 code -
MIM number
Synonym(s) Familial renal glucosuria
SGLT2 deficiency

Summary

Renal glucosuria (RG) is a rare autosomal recessive condition characterized by renal glucose wasting in the absence of hyperclycemia or other forms of tubular dysfunction. The prevalence is unknown. It is caused by mutations in the SLC5A2 gene encoding the sodium/glucose cotransporter type 2 (SGLT2). RG is a benign condition with no symptoms or serious consequences, and does not require a specific therapy. *Author: Orphanet (June 2006)*.

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