Long-term outcome in a case series of Denys–Drash syndrome

BACKGROUND: Denys–Drash syndrome (DDS) is a rare disease caused by mutations in exons 8 and 9 of the WT1 gene. It is characterized by the association of early onset steroid-resistant nephrotic syndrome (SRNS), Wilms’ tumour and, in some patients, intersex disorders, with increasing risk of gonadobla...

Descripción completa

Detalles Bibliográficos
Autores principales: Roca, Neus, Muñoz, Marina, Cruz, Alejandro, Vilalta, Ramon, Lara, Enrique, Ariceta, Gema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Inherited Kidney Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885669/
https://www.ncbi.nlm.nih.gov/pubmed/31807296
http://dx.doi.org/10.1093/ckj/sfz022

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885669/
https://www.ncbi.nlm.nih.gov/pubmed/31807296
http://dx.doi.org/10.1093/ckj/sfz022

Ejemplares similares