Genetic Testing
EMPOWERING WOMEN TO MAKE INFORMED DECISIONS ABOUT THEIR FUTURE
Testing your genetics can discover a genetic mutation that may run in your family, allowing professionals to treat it before any symptoms form. These results can drive individuals toward prevention, monitoring, and treatment options. These approaches can help eliminate the need for more intensive treatment later in the process.
Importance of Genetic Testing
The results can also help parents determine the chances of their current or future child developing a certain family condition.
Prenatal Genetic Testing
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NIPT (Panorama): A noninvasive prenatal test that analyzes fetal DNA to screen for chromosomal conditions such as Down syndrome.
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Amniocentesis: A diagnostic test that analyzes amniotic fluid to detect genetic or chromosomal conditions.
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Chorionic Villus Sampling (CVS): Involves testing placental tissue to identify potential genetic abnormalities early in pregnancy.
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Alpha-fetoprotein (AFP): A maternal blood test that measures AFP levels, which can indicate neural tube defects or, in some cases, cancer.
Carrier Screening
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Horizon Test: Conducted before or during pregnancy to determine whether you carry genes that could be passed on to your child, potentially causing inherited genetic conditions.
Cancer Risk Assessment
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Hereditary Cancer Screening: Identifies inherited genetic mutations that increase your risk for certain cancers. Especially recommended if you have a family history of early-onset or multiple cancers.
Ovarian Cancer Risk
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OVA-1 Test: A blood test that calculates an ovarian malignancy risk score. An abnormal result does not confirm cancer, but may prompt referral to a specialist before surgical decisions are made.
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