Sancakli, O.Kulu, B.Sakallioglu, O.2019-06-282019-06-28201803250075https://www.sap.org.ar/docs/publicaciones/archivosarg/2018/v116n3a22e.pdfhttp://hdl.handle.net/11727/3736Dent's disease is a rare X-linked recessive tubulopathy characterized by low molecular weight (LMW) proteinuria, hypercalciuria, nephrolcalcinosis or nephrolithiasis, proximal tubular dysfunction and renal failure in adulthood. Females are carriers and usually mildly affected. Progression to end-stage renal failure are at the 3rd-5th decades of life in 30-80% of affected males. In the absence of therapy targeting for the molecular defect, the current care of patients with Dent’s disease is supportive, focusing on the prevention of nephrolithiasis and nephrocalcinosis. We present an 11-year-old child with nephrocalcinosis and nephrolithiasis caused by a new mutation at CLCN5 gene. © 2018 Sociedad Argentina de Pediatria. All rights reserved.enginfo:eu-repo/semantics/openAccessCLCN5Dent's diseaseNephrocalcinosisNephrolithiasisProximal renal tubular dysfunctionArticle1163e442e4440004340102000222-s2.0-85048510636