| Literature DB >> 19444483 |
Sidharth Kumar Sethi1, Michael Ludwig, Madhulika Kabra, Pankaj Hari, Arvind Bagga.
Abstract
Dent's disease is an X-linked renal tubular disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrocalcinosis or nephrolithiasis. The disease is caused by mutations in a renal chloride channel gene, CLCN5. We report on three boys, of Indian origin, with Dent's disease that presented at an early age (1-4 years), with polyuria, polydipsia, salt craving, recurrent vitamin A-responsive night blindness, hypophosphataemic rickets, hypercalciuria and low molecular weight proteinuria. All these patients were found to have novel mutations in the CLCN5 gene.Entities:
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Year: 2009 PMID: 19444483 DOI: 10.1007/s00467-009-1198-6
Source DB: PubMed Journal: Pediatr Nephrol ISSN: 0931-041X Impact factor: 3.714