The field of genetics is rapidly changing. As the blueprint of your body, genes are made up of DNA and play an important role in the cause of many illnesses. By studying DNA and its interaction with the environment, genetic counselors can help determine how genes influence health and responses to treatment.
Genetic counseling and testing is right for you if you are concerned about genetic conditions that run in your family and/or are planning a pregnancy. Avera genetic counselors will help you understand the benefits of genetic testing, and help you understand your results. Genetic testing may be an option for you within these specialties:
- Cancer
- Obstetrics and maternal-fetal medicine
- Cardiology
- Neurology
Types of Genetic Counseling
Knowing your own genetic risk for diseases is helpful if you have a personal or family history of disease, including cancer, or would like to plan for a pregnancy.
Expecting Parents
As you think of starting or expanding your family, you may be concerned about inherited or sporadic genetic disorders. Working with Avera’s team of experts who specialize in prenatal genetic testing and counseling, you’ll learn about:
- Your risk of passing genetic disorders
- The nature of these genetic disorders
- Options to manage, prevent or reduce them
- Risk factors of concern unrelated to genetic tendencies
- Methods of preparation for test results
- Prenatal care services that can help you care for children who may have special needs
You can find out your carrier status for a range of health conditions, if you want or need this information.
Learn More
Cancer Risk
If you’ve wondered about your risk for cancer, or your kids’ risk, talk to a genetic counselor at Avera Cancer Institute to find answers to your questions. During the visit, you’ll receive the information you need to make future health care decisions about cancer screening and genetic testing. Through a genetic test, you and your providers may gain insight to determine how to better prevent cancer or catch it in its earliest stages.
Common examples include mutations of the BRCA1 or BRCA2 genes which cause a higher risk for breast and ovarian cancers. Or, gene mutations for Lynch syndrome, which predisposes people to colon and endometrial cancers.
See Details