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• W4327906129 endingPage "215" @default.
• W4327906129 startingPage "205" @default.
• W4327906129 abstract "Germline mutations in tumor suppressor genes and oncogenes lead to hereditary renal cell carcinoma (HRCC) diseases, characterized by a high risk of RCC and extrarenal manifestations. Patients of young age, those with a family history of RCC, and/or those with a personal and family history of HRCC-related extrarenal manifestations should be referred for germline testing. Identification of a germline mutation will allow for testing of family members at risk, as well as personalized surveillance programs to detect the early onset of HRCC-related lesions. The latter allows for more targeted and therefore more effective therapy and better preservation of renal parenchyma." @default.
• W4327906129 created "2023-03-21" @default.
• W4327906129 creator A5038992904 @default.
• W4327906129 date "2023-05-01" @default.
• W4327906129 modified "2023-10-10" @default.
• W4327906129 title "Diseases of Hereditary Renal Cell Cancers" @default.
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