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Conditions We Treat: BRCA1 and BRCA 2 Gene Mutations
Everyone has BRCA1 and BRCA2 genes. Harmful changes (mutations) in one or both of these genes can increase a woman’s risk of developing both breast and ovarian cancers, and in some cases fallopian tube and/or peritoneal cancers. If you have mutations in either of these genes, there are preventive treatment options available to help you reduce your risk.
BRCA1 and BRCA2 Genes: What You Need to Know
- Everyone has BRCA1 and BRCA2 genes. These are important genes that help repair damaged DNA.
- Harmful changes (mutations) in one or both of these genes may increase a woman’s chances of developing breast and ovarian cancer, and in some cases fallopian and/or peritoneal cancer.
- BRCA1 and BRCA2 gene mutations are hereditary and can be passed on to both males and females.
- Genetic testing can reveal BRCA1 and BRCA 2 mutations. If genetic testing determines the presence of BRCA1 and/or BRCA 2 gene mutations, a woman, along with the help of her doctor, can take steps to manage her risk of developing cancer.
- If you are considering undergoing genetic testing, you should first make an appointment with a genetic counselor and a gynecologic oncologist.
Why choose Johns Hopkins for management of BRCA1 and BRCA2 gene mutations?
Rely on the expertise of our physicians to help you manage BRCA1 and BRCA2 gene mutations.
Our Patient Care
We believe in treating the whole patient — body, mind and spirit. “We are by your side every step of the way — whether you are just beginning treatment or have completed treatment and are undergoing survivorship care.” – Amanda Fader, M.D.
As part of your care, we offer a range of fertility preservation services.