Genetic Risk and Hereditary Cancers
Sessions may also consider multigene panels covering BRCA1, BRCA2, PALB2, CHEK2, ATM, and mismatch-repair genes, together with their varying levels of risk. Presentations will examine risk-prediction models, polygenic risk scores, and population-based testing in selected settings. Researchers will discuss cascade testing, family communication, and the growing role of genetic counsellors supported by telehealth. Attention will be given to variants of uncertain significance, periodic reanalysis, and clear reporting standards. Privacy, insurance discrimination, direct-to-consumer testing, and consent for data sharing will be addressed. Surveillance protocols, the timing of risk-reducing surgery, and chemoprevention in carriers will be reviewed with attention to quality of life. Cultural and religious perspectives on inherited risk will also be considered.
Related Conference of Genetic Risk and Hereditary Cancers
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