Patient Resources

Patients seeking additional information on a wide range of topics can find information at
The American College of Obstetrics and Gynecology Patient Information Page

Natera Genetic Testing Options Performed at Lee OBGYN

Panorama™

Noninvasive prenatal testing (NIPT)

For more information, visit
https://www.natera.com/womens-health/panorama-nipt-prenatal-screening/

Panorama™ is a blood-based genetic, prenatal screening test of the pregnant person that screens for common chromosomal conditions that affect a baby’s health. Panorama™ uses SNP*-based technology to deliver highly accurate results and unique insights for both singleton and twin pregnancies.

Panorama™ can be performed as early as nine weeks gestation. Most results will be returned to your doctor within 5-7 calendar days from the date that samples are received.

Panorama™ is a screening test, which means that this test does not make a final diagnosis. A high risk result means that your pregnancy has a higher chance of having a specific genetic condition. However, you cannot know for sure if your baby has that condition based upon the screening result alone. All medical decisions should be made after discussion with your healthcare provider regarding diagnostic testing during the pregnancy, like chorionic villus sampling (CVS) or amniocentesis, or testing the baby after birth.

Horizon™

Carrier Screening to determine risk of passing on genes

For more information, visit
https://www.natera.com/womens-health/horizon-advanced-carrier-screening/

Horizon genetic carrier screening helps couples determine the risk of passing on serious genetic conditions to their child. Carrier screening can be performed either before or during pregnancy. All of us are carriers of at least one genetic condition.1 Most carriers are healthy with no family history, but they are at risk of passing on a genetic condition to their child. Carrier screening is a genetic test that identifies if you carry a gene with a change, or variant, that can impact your child. When performed before conceiving, genetic carrier screening can provide actionable knowledge and the opportunity to pursue alternative reproductive options. Carrier screening during pregnancy can help couples decide on prenatal or infant diagnostic testing, and if necessary, help them prepare emotionally, medically, and financially for a baby affected by a genetic condition. It is common for people to be carriers of at least one genetic condition.1 Most carriers are healthy with no family history, but they are at risk of passing on a genetic condition to their child. Horizon carrier screening is a genetic test performed before or during pregnancy that identifies if you carry a gene with a change, or variant, that can impact your child.

Empower™

Hereditary cancer testing, made accessible

For more information, visit https://www.natera.com/oncology/empower-hereditary-cancer-test/

Empower is a genetic test for those who want to know more about their risk of developing cancer, why it might be common in their family, or want to inform treatment options following a cancer diagnosis.

Empower screens for genes associated with increased risk for common hereditary cancers. Our Empower multi-cancer panels include commonly screened-for genes associated with 12+ types of cancer.

Cancer previvors are healthy people who know they inherited a high risk for cancer, and can take action to lower their risk. Genetic risk for certain cancers runs in families, dramatically increasing a person’s lifetime risk for developing cancer. If you know you’re at risk, you can take steps to get ahead of cancer.

The Empower™ Hereditary Cancer Test screens your DNA for a wide range of gene variants that are known to impact risk for multiple kinds of cancer. Ask your clinician if Empower is right for you and your family.

Anora™

Highly comprehensive miscarriage test

For more information, visit
https://www.natera.com/womens-health/anora-miscarriage-test/

A miscarriage can be devastating. You are left to grieve and wonder why. Your pain and fear can make it more difficult to move ahead, and you want answers.

Anora helps determine why a miscarriage occurred. Testing is performed on tissue from the pregnancy loss.

Anora tests for chromosomal abnormalities and results are typically returned to your doctor within one week of sample receipt. The results obtained from chromosome testing after a miscarriage can reduce your emotional burden and improve your chances of a future successful pregnancy. If genetic testing identifies a chromosomal abnormality as the cause, your chances of recurrence are low. Genetic testing can save your provider from performing costly medical work-up to determine the cause of miscarriage.