The Importance of Breast Cancer Genetic Testing for Women

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Breast Cancer Genetic Testing

Tumor & Cancer-The Importance of Breast Cancer Genetic Testing for Women – What is Breast Cancer Genetic Testing? This is a test that looks for specific mutations changes in someone’s genes, chromosomes, or proteins.

Genetic mutations can possibly beneficial, harmful, uncertain effects, or no effect aka neutral on health. When mutations show as harmful, it can increase a person’s chance or risk of having disease of breast cancer.

But, inherited mutations are happened in about 5 to 10 percent of all cancers including breast cancer.

Even if it is not caused by an inherited mutation, breast cancer can sometimes appear in every women or run in women relatives in families.

For example, when a daughter shared environment or lifestyle with her mother such as tobacco use, it can cause breast cancer to develop among female members in family.

The genetic mutations which cause breast cancer has been identified. And the condition can be confirmed whether is, indeed, the result of an inherited syndrome by breast cancer genetic testing.

For example, when a daughter shared environment or lifestyle with her mother such as tobacco use, it can cause breast cancer to develop among female members in family.

The genetic mutations which cause breast cancer has been identified. And the condition can be confirmed whether is, indeed, the result of an inherited syndrome by breast cancer genetic testing.

It also can determine whether our family member without noticeable disease inherited the same mutation as the family member who carry a cancer mutation.

The person’s risk of developing cancer can increase when they inherited genetic mutations. But it is also depends on the function of the gene. The increasing of cancer risk is associated with mutation in genes which repair damaged DNA and control cell growth.

How is Breast Cancer Genetic Testing Done?

Usually, the person’s doctor or other health care provider will request the genetic tests. It may be possible for us to do some genetic tests without doctor or health care provider’s order.

But this method is not recommended because you can’t get the valuable opportunity to discuss the result and complicated decision with someone who professional and knowledgeable in this area.

The test is done with a small sample of tissue or fluid. Usually, blood is used in the test as well as saliva, skin cells, cells from inside the cheek, or amniotic fluid which is the fluid surrounding a developing fetus.

Then your sample will be send to a laboratory which focuses in genetic testing. After that, the test result will be returns from the laboratory to the doctor or genetic counselor that request the genetic test. But sometimes, in

But sometimes, in certain laboratory, they will send the result directly to the patient. Usually the test takes several weeks or it can be longer to get the test result. It is recommended to do counseling with doctor or health care provider both before and after genetic testing.

This counseling done to make sure that the patient have accurate information about the result of genetic test and get the information about their health and care.

Who Can Help People Understand Their Breast Cancer Genetic Testing’s Results?

A doctor, genetic counselor, or other health care provider and professional trained in genetic will help the patient or the family to understand the result of their genetic test.

The counseling will include discussing recommendations for treatment and preventive care. They will also give other information and providing emotional support to the patient.

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Someone who likes to share information about health. Especially regarding cancer and tumor diseases. Health is a gift that is extraordinary.