
Safe and accurate screening for chromosomal conditions
Watch this informative video to learn more about Non-Invasive Prenatal Testing and how it can help assess your baby's health.
Non-Invasive Prenatal Testing (NIPT) is a safe and accurate blood test that analyzes small fragments of fetal DNA circulating in the mother's blood. It screens for common chromosomal conditions without any risk to the pregnancy.
Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13)
Turner syndrome, Klinefelter syndrome, and other sex chromosome abnormalities
Myth:
NIPT is the same as amniocentesis.
Fact:
NIPT is a simple blood test with no risk to the pregnancy, while amniocentesis is an invasive procedure with a small risk of complications.
Myth:
NIPT can diagnose all genetic conditions.
Fact:
NIPT screens for common chromosomal conditions but cannot detect all genetic disorders or structural abnormalities.
Myth:
NIPT is only for high-risk pregnancies.
Fact:
NIPT is available to all pregnant women and can provide valuable information regardless of risk factors.
Myth:
NIPT results are always 100% accurate.
Fact:
While NIPT is highly accurate, no test is perfect. Positive results should be confirmed with diagnostic testing.
NIPT is highly accurate, with detection rates of over 99% for common chromosomal conditions. However, it is a screening test, not a diagnostic test.
Coverage varies by insurance provider and individual circumstances. We can help you verify your coverage before testing.
If results indicate a high risk for a condition, we will provide genetic counseling and discuss options for confirmatory testing.
Yes, NIPT can be performed for twin pregnancies, though the accuracy may vary depending on the type of twins.
Results are typically available within 7-10 business days after the blood draw.
Take the first step towards understanding your baby's health with our expert team.
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