Wilms' tumor risk factors
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shanshan Cen, M.D. [2]
Overview
The risk factors of wilms' tumor include family history, congenital anomalies, and associated syndromes.
Risk factors
- Familial Wilms tumor [1]
- Congenital anomaly
- Hemihyperplasia
- Urinary tract anomalies, including cryptorchidism and hypospadias
- Aniridia
- WT1-related syndromes include the following:
- WAGR syndrome
- Denys-Drash syndrome and Frasier syndrome
- WT2-related syndromes include the following:
- Beckwith-Wiedemann syndrome
- Other syndromes include the following:
- Perlman syndrome.
- Simpson-Golabi-Behemel syndrome
- Sotos syndrome
- 9q22.3 microdeletion syndrome
- Bloom syndrome
- Li-Fraumeni syndrome
- Alagille syndrome
References
- ↑ National Cancer Institute. Physician Data Query Database 2015. http://www.cancer.gov/publications/pdq