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Ovarian Cancer and Genetics – Oren Zarif

oren by oren
June 2, 2022
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The genes in our body are what makes us who we are, and it’s possible that some of our genes are faulty or defective, which can result in different types of cancer. Inheritance of certain genes is often inherited, but some can also be changed over time. A common faulty gene is BRCA1, which causes ovarian cancer. A faulty gene can affect many organ systems, including the brain. Genetic changes are associated with an increased risk of developing ovarian cancer, so understanding what causes your genetic makeup can help you choose the right treatment.

Some risk factors for ovarian cancer include genetic disorders, and being older than 60 can increase your risk. Genetic factors account for between 10% and 15% of ovarian cancer cases. The risk of getting the disease can be reduced by having children, but it’s important to remember that not everyone who has one of these risk factors will develop it. For those who are at risk, it’s always best to discuss your risk factors with a health care provider.

Ovarian cancer is a condition where the tumors in the ovaries spread to other organs in the pelvic region. It can spread to the fallopian tubes and uterus, and it can also affect the lymph nodes or abdominal fluid. This cancer affects both women and transgender men. For those who were born as a female, ovarian cancer should be considered a serious health concern.

Symptoms of ovarian cancer can include sudden, unexplained weight loss and abdominal pain. These symptoms usually do not go away on their own and should be addressed by a medical professional as soon as possible. A health care provider can help you find a doctor in your area. If you’re not sure who to consult with, you can try Healthline’s FindCare tool to find a primary care doctor in your area.

Germ cell ovarian cancer is rare and occurs in about two percent of all cases. The survival rate for women diagnosed with this type of ovarian cancer is approximately nine out of 10 years after diagnosis. The tumor can be benign or cancerous, and can grow rapidly. While early stages of ovarian cancer may be difficult to detect, most patients will live for five years or more with treatment. It’s important to be aware of possible symptoms because it can occur at any age.

Many types of cancer have screening tests to detect pre-cancers and cancer at its early stages. Early detection is critical, as the cancer is easier to cure. By having a screening test done regularly, you will be more likely to be diagnosed early and receive treatment for your disease. If you have persistent symptoms, consult a healthcare provider. They may be able to identify the problem. There are no symptoms of ovarian cancer in the early stages, but if you have a family history of this gene, it’s still important to get a regular pelvic examination.

Pap smear tests can detect ovarian cancer. However, these tests are not reliable and are only effective for women at high risk for the disease. Women who have genetic risk factors for this disease should ask their doctors about genetic testing or other screening tests. In general, women should undergo annual pelvic exams to ensure regular gynecological care. Even if you don’t have a family history of this disease, a pelvic exam should be scheduled.

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