Living With Brca Mutations: Family Communication and Reproductive Choices

Breast cancer is a multifactorial disease with a significant genetic component, particularly related to BRCA1/2 mutations, which markedly increase the risk of breast and ovarian cancers. The identification of a pathogenic variants carries clinical, preventive, and psychological implications, that extend to family members. Oncogenetic counseling plays a central role in identifying at-risk individuals, guiding decision-making, and supporting psychological well-being. This article explores the communication of the diagnosis within families, coping with cancer risk, and fertility management in young women.