biostudies-literatureUnknown16(1)Leggatt GDent disease type 1 is suspected in the presence of a complete phenotype of low molecular weight (LMW) proteinuria, hypercalciuria and at least one of the following: nephrocalcinosis, nephrolithiasis, haematuria, hypophosphatemia or chronic kidney disease (CKD). We present two brothers who presented with CKD alone. In the absence of typical clinical features, further assessment of LMW proteinuria and hypercalciuria was not undertaken. Whole-genome sequencing revealed hemizygous loss of function mutations in chloride voltage-gated channel 5 (<i>CLCN5)</i> consistent with Dent disease. Dent disease should, therefore, be considered in patients with an incomplete phenotype, including unexplained CKD alone.Clinical kidney journal192-194https://www.ebi.ac.uk/biostudies/studies/S-EPMC9871842biostudies-literatureHemizygous loss of function mutations in <i>CLCN5</i> causing end-stage kidney disease without Dent disease phenotype.PMC9871842Ennis SVeighey KLeggatt GGilbert RDRahman TGast CfalseHemizygous loss of function mutations in <i>CLCN5</i> causing end-stage kidney disease without Dent disease phenotype.Dent disease type 1 is suspected in the presence of a complete phenotype of low molecular weight (LMW) proteinuria, hypercalciuria and at least one of the following: nephrocalcinosis, nephrolithiasis, haematuria, hypophosphatemia or chronic kidney disease (CKD). We present two brothers who presented with CKD alone. In the absence of typical clinical features, further assessment of LMW proteinuria and hypercalciuria was not undertaken. Whole-genome sequencing revealed hemizygous loss of function mutations in chloride voltage-gated channel 5 (<i>CLCN5)</i> consistent with Dent disease. Dent disease should, therefore, be considered in patients with an incomplete phenotype, including unexplained CKD alone.2023-01-01T00:00:00Z2023 Jan2025-04-22T18:16:06.592Z2025-04-06T02:20:56.511ZS-EPMC98718423672644110.1093/ckj/sfac127