Expanding the phenotype of proteinuria in Dent disease. A case series

Academic Article


  • Background: Dent disease is an X-linked recessive renal tubular disorder characterized by low molecular weight proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, and progressive renal failure (MIM 300009). A recent case series identified four patients with CLCN5 mutations who presented with nephrotic-range proteinuria, histologic evidence of focal segmental and/or global sclerosis, and low molecular weight proteinuria.
  • Published In

    Digital Object Identifier (doi)

    Author List

  • Cramer MT; Charlton JR; Fogo AB; Fathallah-Shaykh SA; Askenazi DJ; Guay-Woodford LM
  • Start Page

  • 2051
  • End Page

  • 2054
  • Volume

  • 29
  • Issue

  • 10