Spectrum of Clinical Manifestations in Children With WT1 Mutation: Case Series and Literature Review

BACKGROUND: Mutations of the Wilms tumor suppressor-1 gene (WT1) are associated with life-threatening glomerulopathy, disorders of sexual development, Wilm's tumor, and gonadal malignancies. Our objectives were to describe the clinical presentations, age of progression, and onset of complicatio...

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Detalles Bibliográficos
Autores principales: Arroyo-Parejo Drayer, Patricia, Seeherunvong, Wacharee, Katsoufis, Chryso P., DeFreitas, Marissa J., Seeherunvong, Tossaporn, Chandar, Jayanthi, Abitbol, Carolyn L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051246/
https://www.ncbi.nlm.nih.gov/pubmed/35498778
http://dx.doi.org/10.3389/fped.2022.847295

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051246/
https://www.ncbi.nlm.nih.gov/pubmed/35498778
http://dx.doi.org/10.3389/fped.2022.847295

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