Genetic Testing

Genetic Testing

Genetic testing is optional and available to all patients. In some cases, a patient's personal or family history may lead the doctor to recommend specific tests.

First Trimester Screening (Starting at 10 Weeks)

This screening assesses your baby's risk for Down syndrome and certain spinal cord defects. It is entirely optional and can be performed if you and your doctor decide to proceed.

Cystic Fibrosis (CF) Screening (First Visit)

Cystic fibrosis (CF) is a genetic disorder that affects digestion and breathing. It is usually diagnosed in early childhood. Testing is available to determine whether you are at increased risk of passing CF to your child.

• You will find a Mayo Clinic pamphlet in your welcome bag with additional details.

• You will be asked to sign a consent form indicating whether you choose to proceed with testing.

• Check with your insurance provider to confirm if this test is a covered benefit.

Quad Screen (16-22 Weeks)

The AFP (Alpha-Fetoprotein) test is available between 16-20 weeks of pregnancy to help identify the risk of certain birth defects.

• A Mayo Clinic pamphlet in your welcome bag provides further explanation.

• You will need to sign a consent form indicating whether you choose to proceed.

• Results typically take about 7 days.

• Check with your insurance provider to determine coverage.

Additional Genetic Testing

Depending on your family history, further genetic testing may be recommended. This could include:
✔ Genetic counseling
✔ Ultrasound evaluations
✔ Amniocentesis

If you have any questions about genetic testing options, please discuss them with your doctor at your next visit.