Discover the Benefits of Non-Invasive Prenatal Testing (NIPT) for All Pregnancies

This test includes:

Trisomy 21 (Down Syndrome)

Trisomy 18 ( Edwards Syndrome)

Trisomy 13 (Patau Syndrome)

Fetal sex determination

Additional options available. Please ask your healthcare provider for details.

Who is this test for?

This panel is for anyone who seeks more information about the genetic health of their unborn child.

Process and Results

This test is performed by taking a routine blood draw (7-10mL) from the mother.

Results can be expected within 5-7 days of our receipt of the sample.

Results will be available on our online portal, please ask your provider for details.

Non-Invasive Prenatal Testing (NIPT) is a safe and convenient genetic screening test that provides dependable results to help expecting parents make informed decisions about their pregnancy and the health of their baby.

NIPT uses a simple maternal blood draw to analyze fetal DNA (cfDNA) for common chromosomal abnormalities, such as Down syndrome, trisomy 18, and trisomy 13 as well as others. With high accuracy and lower risk than other methods, NIPT offers valuable information to help you make informed decisions about your pregnancy.

NIPT can be performed as early as 10 weeks gestation and is recommended for all pregnant mothers by the American College of Obstetrics and Gynecologists. Our NIPT test is suitable for both single and twin pregnancies, providing accurate and reliable results to help you better understand the genetic health of your baby or babies.

Our team of experienced genetic counselors can review any significant results and go over next steps. Speak to your healthcare provider about NIPT and how it can provide important insights into your baby's health.

Stay ahead of your baby's health