11/03/2025
About 5–10% of breast cancer cases are linked to inherited genetic mutations, particularly in the BRCA1, BRCA2, and PALB2 genes. These mutations impair the body’s ability to repair damaged DNA, allowing abnormal cells to grow unchecked. Women with a strong family history — like a mother, sister, or daughter diagnosed before age 50 — face a higher lifetime risk. Men can also carry and pass on these mutations. Genetic counseling and testing can help identify carriers and guide preventive steps such as earlier screening, MRI monitoring, or even risk-reducing medication. Knowing your family history empowers you to detect problems early — when treatment is most effective.