Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience

Hol JA, Jongmans MCJ, Sudour-Bonnange H, Ramirez-Villar GL, Chowdhury T, Rechnitzer C, Pal N, Schleiermacher G, Karow A, Kuiper RP, De Camargo B, Avcin S, Redzic D, Wachtel A, Segers H, Vujanic GM, Van Tinteren H, Bergeron C, Pritchard-Jones K, Graf N, Van Den Heuvel-Eibrink MM (2020)


Publication Type: Journal article

Publication year: 2020

Journal

DOI: 10.1002/cncr.33304

Abstract

Background WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays) is a rare contiguous gene deletion syndrome with a 45% to 60% risk of developing Wilms tumor (WT). Currently, surveillance and treatment recommendations are based on limited evidence.

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How to cite

APA:

Hol, J.A., Jongmans, M.C.J., Sudour-Bonnange, H., Ramirez-Villar, G.L., Chowdhury, T., Rechnitzer, C.,... Van Den Heuvel-Eibrink, M.M. (2020). Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience. Cancer. https://dx.doi.org/10.1002/cncr.33304

MLA:

Hol, Janna A., et al. "Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience." Cancer (2020).

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