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Wilms tumor is a rare kidney cancer that is usually diagnosed in children under the age of six. Wilms tumor is mostly the result of aberrations in WT1 gene, located on chromosome 11p13. In addition to being a risk factor for Wilms tumor, WT1 aberrations cause extra renal complications and other malignancies. This book brings together the basic and clinical aspects of Wilms tumor and WT1 research under three sections. Section I provides a comprehensive guide to the epidemiology, diagnostics, management, and treatment of Wilms tumor. Section II covers the biological aspects of Wilms tumor and WT1. Section III focuses on the role of WT1 in cardiac development, prostate cancer, glioblastoma and minimal residual disease.
Contributors: 64; Chapters: 16; Figures: 50; Tables: 20; Pages: 294
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Copyright © 2016 Codon Publications.
Published under Creative Commons Attribution 4.0 International (CC BY 4.0). Users are allowed to share (copy and redistribute the material in any medium or format) and adapt (remix, transform, and build upon the material for any purpose, even commercially), as long as the authors and the publisher are explicitly identified and properly acknowledged as the original source.
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This book focuses on Childhood Cancer, specifically Wilms Tumor. It is the work of 64 contributors and has been written to cover diagnosis and treatment of the disease with modern techniques. This is written for Oncologists, Hematologists and Pathologists.
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Feedback?December 20, 2017 | Edited by openaccessresearcher | Metatag |
December 15, 2017 | Edited by openaccessresearcher | NCBI linked publication |
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December 15, 2017 | Created by openaccessresearcher | Added new book. |