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

• Asıl Yazarlar: Patricia Arroyo-Parejo Drayer (Yazar), Wacharee Seeherunvong (Yazar), Chryso P. Katsoufis (Yazar), Marissa J. DeFreitas (Yazar), Tossaporn Seeherunvong (Yazar), Jayanthi Chandar (Yazar), Carolyn L. Abitbol (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Frontiers Media S.A., 2022-04-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

BackgroundMutations 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 complications...