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• W2012210392 abstract "Dent's disease is an X-linked hereditary renal tubular disorder characterized by low-molecular-weight proteinuria (LMWP), hypercalciuria, nephrocalcinosis, nephrolithiasis, rickets and progressive renal failure. About 60% of patients have mutations in the CLCN5 gene (Dent 1), which encodes a kidney-specific chloride/proton antiporter, and 15% of patients have mutations in the OCRL1 gene (Dent 2). The aim of the study was to identify CLCN5 mutations in Jewish Israeli families with Dent's disease and to characterize the associated clinical syndromes. We studied 17 patients from 14 unrelated Israeli families with a clinical diagnosis of Dent's disease. LMWP was detected in all patients. Most of the affected individuals had hypercalciuria and nephrocalcinosis. Renal stones were found in 1 patient, and renal insufficiency developed in 2 patients. We identified six different truncating CLCN5 mutations that were segregated with the disease in 7 families: three nonsense mutations (Arg28stop, Arg467stop and Arg637stop), one deletion mutation (505delA) and two novel mutations, consisted of one deletion mutation (1493delG) and one insertion mutation (409insC). All the mutations cause premature termination of protein translation and result in a non-functional truncated protein. The clinical characteristics of patients with different mutations were, in general, similar." @default.
• W2012210392 created "2016-06-24" @default.
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• W2012210392 date "2009-06-16" @default.
• W2012210392 modified "2023-09-30" @default.
• W2012210392 title "Truncating Mutations in the Chloride/Proton <i>ClC-5</i> Antiporter Gene in Seven Jewish Israeli Families with Dent’s 1 Disease" @default.
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• W2012210392 doi "https://doi.org/10.1159/000224793" @default.
• W2012210392 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19546586" @default.
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