Denys-Drash Syndrome (DDS) Latest Advances

Find the Latest Research About Denys-Drash Syndrome (DDS)

Last Updated: 06/30/2026

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Found 425 publications

Case Report: Neonatal nephropathy with polycystic appearance in child harboring WT1 variant.

Case Report: Neonatal nephropathy with polycystic appearance in child harboring WT1 variant.

Journal: Frontiers in pediatrics
Published: August 26, 2025

Denys-Drash Syndrome by WT1 Gene: Clinical Variability and Management Challenges in Two Saudi Infants.

Denys-Drash Syndrome by WT1 Gene: Clinical Variability and Management Challenges in Two Saudi Infants.

Journal: Case reports in endocrinology
Published: July 30, 2025

Corrigendum to "Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children" [Kidney International Reports Volume 10, Issue 4, April 2025, Pages 1205-1212].

Corrigendum to "Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children" [Kidney International Reports Volume 10, Issue 4, April 2025, Pages 1205-1212].

Journal: Kidney international reports
Published: July 18, 2025

Familial WT1-associated nephropathy - 46, XY Frasier syndrome and 46, XX steroid-resistant nephrotic syndrome in female siblings: A case report and review of literature.

Familial WT1-associated nephropathy - 46, XY Frasier syndrome and 46, XX steroid-resistant nephrotic syndrome in female siblings: A case report and review of literature.

Journal: World journal of nephrology
Published: June 20, 2025

Reconciling Oncologic Outcomes With Renal Preservation in Denys-Drash Syndrome and Recurrent Wilms Tumor: A Case-Based Discussion.

Reconciling Oncologic Outcomes With Renal Preservation in Denys-Drash Syndrome and Recurrent Wilms Tumor: A Case-Based Discussion.

Journal: Urology
Published: June 12, 2025

Sacral Erector Spinae Plane Block for Hypospadias Surgery in a Patient With Denys-Drash Syndrome: A Case Report.

Sacral Erector Spinae Plane Block for Hypospadias Surgery in a Patient With Denys-Drash Syndrome: A Case Report.

Journal: A&A practice
Published: June 02, 2025

WT1-Related Nephropathy in a Phenotypically Female Child: A Case of Clinical and Genetic Discordance.

WT1-Related Nephropathy in a Phenotypically Female Child: A Case of Clinical and Genetic Discordance.

Journal: Children (Basel, Switzerland)
Published: March 20, 2025

Novel WT1 and ACTN4 co-mutations in a patient with Denys-Drash syndrome and an atypical, potentially attenuated presentation of nephropathy: a case report.

Novel WT1 and ACTN4 co-mutations in a patient with Denys-Drash syndrome and an atypical, potentially attenuated presentation of nephropathy: a case report.

Journal: BMC nephrology
Published: March 03, 2025

Congenital nephrotic syndrome in a newborn with glycogen storage disease and Wilms tumor 1 (WT1) mutation.

Congenital nephrotic syndrome in a newborn with glycogen storage disease and Wilms tumor 1 (WT1) mutation.

Journal: CEN case reports
Published: February 15, 2025

Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children.

Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children.

Journal: Kidney international reports
Published: December 17, 2024

Paediatric renal tumors: An insight into molecular characteristics, histomorphology and syndromic association.

Paediatric renal tumors: An insight into molecular characteristics, histomorphology and syndromic association.

Journal: World journal of nephrology
Published: July 21, 2024

A review of the genetic background in complicated WT1-related disorders.

A review of the genetic background in complicated WT1-related disorders.

Journal: Clinical and experimental nephrology
Published: May 07, 2024
Showing 1-12 of 425

Last Updated: 06/30/2026