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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

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