Breast Cancer and Genetics
The two most common genetic risk factors for breast cancer are the BRCA1 & BRCA2 genes. Approximately 5% of all breast cancers are caused by a recognised specific genetic predisposition due to germ line mutations of one of two different genes: BRCA1 located on Chromosome 17q, BRCA2 located on Chromosome 13q. BRCA1 mutations also predispose to carcinoma of the ovary and possibly carcinoma of the Fallopian tube. The risk of developing breast cancer among carriers is around 55% by age 70. BRCA2: The product of BRCA2 is involved in controlling gene function and DNA repair.
Related Conference of Breast Cancer and Genetics
Breast Cancer and Genetics Conference Speakers
Recommended Sessions
- Breast Cancer Risk Factors
- Breast Cancer
- Breast Cancer and Genetics
- Breast cancer and the Immune system
- Breast Cancer Clinical Trials
- Breast Cancer Nursing
- Breast Cancer Recurrence
- Breast Implants
- Breast Microcalcifications
- Reconstruction of breast cancer
- Surgeries involved in Breast Cancer
- Treating Breast Cancer with Chemotherapy
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