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Caring for patients with breast cancer from 35 hospitals and hospices across london and the home counties 		Call: 020 7830 2323
Open 9am - 5pm
Answerphone at
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Family History

The risks of inheriting an alteration in a breast and/or ovarian cancer gene increase with the strength of the family history and the age at diagnosis.  In a breast screening or cancer genetic clinic it can be determined whether individuals with breast and/or ovarian cancer in their families are at low, moderate or high risk of having a change in their BRCA1 or 2 genes.  The family is placed into these three categories depending on:

  • The number of relatives (on the same side of the family) with breast and/or ovarian cancer
  • The age of onset of the cancer (individuals are at higher risk if onset of cancer is at a young age, especially if under 50 years)
  • Whether there is a case of bilateral breast cancer (cancer affecting both breasts) or male breast cancer in a close family member
We are interested in delivering a service to individuals with low, moderate and high-risk family histories.  Those designated with a high risk of having a change in their BRCA1 or 2 genes will be referred to and will be offered genetic testing by their local cancer genetic clinic.  Those designated with moderate risks will be seen and managed in family breast cancer clinics, and primary care providers will see those with low risk family histories.

Genetic versus Sporadic Breast Cancer

Genetics

Genetic Testing

 
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OTHER TESTIMONIALS
“When you came to see me nearly a year ago, I was very receptive to your offers of help. But I could have no idea how much Cancerkin would do for me over this difficult year.”
Gillian
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