Dent Disease Latest Advances

Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.

Journal: DNA and cell biology

Published: April 06, 2026

Clinical variation in Lowe syndrome: what and how?

Journal: Frontiers in cell and developmental biology

Published: October 08, 2025

Bioinformatics analysis of a CLCN5 geneframeshift mutation in a patient with Dent disease.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Published: September 08, 2025

Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine.

Journal: BMC nephrology

Published: September 05, 2025

The Significance of FGF23 and 24,25-Dihydroxyvitamin D in Dent Disease Type 1.

Journal: Clinical journal of the American Society of Nephrology : CJASN

Published: August 04, 2025

Ten tips on the work-up and management of CKD patients with nephrolithiasis.

Journal: Clinical kidney journal

Published: July 21, 2025

Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case Report.

Journal: Case reports in nephrology and dialysis

Published: July 10, 2025

Clinical and genetic analysis of a patient with Dent disease due to hemizygous variant of the CLCN5 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: June 24, 2025

Coexisting genetic kidney disease explains many cases of 'familial' IgA nephropathy where the proband has biopsy-confirmed mesangial IgA deposits.

Journal: Frontiers in medicine

Published: June 16, 2025

Phenotype and genotype analyses of 21 Chinese patients with Dent disease.

Journal: Journal of biomedical research

Published: May 27, 2025

Three intronic variants altering RNA splicing were identified in the CLCN5 gene by minigene assay.

Journal: BMC medical genomics

Published: May 25, 2025

Genetic and clinical phenotype of Dent disease in Chinese children and the etiological analysis of early - onset chronic kidney disease.

Journal: Italian journal of pediatrics

Published: March 26, 2025

Dent Disease Latest Advances

Find the Latest Research About Dent Disease

Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.

Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.

Clinical variation in Lowe syndrome: what and how?

Clinical variation in Lowe syndrome: what and how?

Bioinformatics analysis of a CLCN5 geneframeshift mutation in a patient with Dent disease.

Bioinformatics analysis of a CLCN5 geneframeshift mutation in a patient with Dent disease.

Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine.

Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine.

The Significance of FGF23 and 24,25-Dihydroxyvitamin D in Dent Disease Type 1.

The Significance of FGF23 and 24,25-Dihydroxyvitamin D in Dent Disease Type 1.

Ten tips on the work-up and management of CKD patients with nephrolithiasis.

Ten tips on the work-up and management of CKD patients with nephrolithiasis.

Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case Report.

Dual-Genetic Etiology in an Atypical Dent Disease Phenotype Which Combines Features of Focal Segmental Glomerulosclerosis and Ellis-Van Creveld-Like Syndrome: A Case Report.

Clinical and genetic analysis of a patient with Dent disease due to hemizygous variant of the CLCN5 gene

Clinical and genetic analysis of a patient with Dent disease due to hemizygous variant of the CLCN5 gene

Coexisting genetic kidney disease explains many cases of 'familial' IgA nephropathy where the proband has biopsy-confirmed mesangial IgA deposits.

Coexisting genetic kidney disease explains many cases of 'familial' IgA nephropathy where the proband has biopsy-confirmed mesangial IgA deposits.

Phenotype and genotype analyses of 21 Chinese patients with Dent disease.

Phenotype and genotype analyses of 21 Chinese patients with Dent disease.

Three intronic variants altering RNA splicing were identified in the CLCN5 gene by minigene assay.

Three intronic variants altering RNA splicing were identified in the CLCN5 gene by minigene assay.

Genetic and clinical phenotype of Dent disease in Chinese children and the etiological analysis of early - onset chronic kidney disease.

Genetic and clinical phenotype of Dent disease in Chinese children and the etiological analysis of early - onset chronic kidney disease.