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Breast Cancer Genomic Testing

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BRCA 1 and BRCA2 Genes: What Do Women Need to Know?

Inherited genetic mutations can increase a woman’s risk of developing breast cancer. For instance, a mutation in two of the better-understood genes linked to a substantial increased risk of breast cancer, the BRCA1 and BRCA2 genes, account for up to:

  • 10 percent of all breast cancers.
  • 50 percent of hereditary breast cancers (caused by inherited genetic mutations).

Women with a strong family history of breast cancer should take time to learn how genetic testing is appropriate for them. It is important to remember that risk can be passed down from either your father or mother. A detailed knowledge of the medical history of your relatives can be extremely helpful.

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Breast Cancer Genomics

The availability of molecular information on breast cancer genomics is rapidly expanding. Patients who are newly diagnosed with breast cancer can easily be overwhelmed by volumes of information in a very short period of time. The good news is that all of the information available is meant to guide personal decisions for cancer management so that we use biology and science for real-life choices. Knowledge is power.

Next Generation of Breast Cancer | Dr Kapoor

The Next Generation of Breast Cancer

Join Dr. Kapoor on Thursday, October 9 from 6-7:30 pm in Santa Ana for her talk on advances in screening, surveillance and […]

Dr. John Link on the Breast Cancer Genomic Revolution

Dr. John Link was recently interviewed by the Symphony Sisterhood about the breast cancer genomic revolution that is changing the way we treat breast cancer. Please visit the link to view the minute and a half interview.

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