Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children

Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children

Introduction: Denys-Drash syndrome (DDS) is a rare disease typically associated with a triad of early onset nephrotic syndromes (NS), susceptibility to Wilms tumor (WT), and genitourinary structural defects. DDS is caused by Wilms’ tumor suppression gene (WT1) variants, with the most frequent varian...

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Main Authors: Mathilde Glénisson, Mathilde Grapin, Thomas Blanc, Evgenia Preka, Julien Hogan, Manon Aurelle, Gwenaëlle Roussey, Antoine Mouche, Caroline Rousset-Rouviere, Robert Novo, Camille Faudeux, Marc Fila, Isabelle Vrillon, Sylvie Cloarec, Thomas Simon, Jérôme Harambat, Edouard Martinez Casado, Julien Rod, Morgane Carre Lecoindre, Laurence Heidet, Olivia Boyer, Nicolas Garcelon, Jessica Kachmar, Guillaume Dorval, Sabine Sarnacki
Format: Article
Language:English
Published: Elsevier 2025-04-01
Series:Kidney International Reports
Subjects:
Denys-drash syndrome
Nephrotic syndrome
WT1
Online Access:http://www.sciencedirect.com/science/article/pii/S246802492500021X
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