
What is a NIPT test
A NIPT Test is carried out by simply drawing blood from the mother after 10 weeks into pregnancy. The NIPT Test can reveal the baby’s gender during the first trimester, while traditional ultrasound can reveal the gender during the second trimester.
Safe
Non-invasive screening with no increased risk of miscarriage
Accurate
Detects more than 99% of cases of Down Syndrome
Convenient
A simple blood sample drawn by a nurse who comes to you
Fast
to receive the results
Is NIPT Test necessary?
Frequently Asked Questions about NIPT Test
How accurate are the results of a NIPT test?
Accuracy rates depends on the chromosome.
How does a NIPT test work?
The NIPT test examines cell-free DNA (cfDNA) released from the placenta into the mother’s bloodstream. The NIPT test detects chromosomal abnormalities within this fetal cfDNA present in the mother’s blood, with a simple blood draw.
How do I read the results of a NIPT test?
A NIPT test is a screening test — not a diagnostic test. This means that it can’t diagnose a genetic condition with certainty. It can, however, predict whether the risk of a genetic condition is high or low. Therefore, you need to have the results read by a professional. We strongly recommend you to take the results to your OBGYN to interpret the results.
Who should get a NIPT test?
Any pregnant women could get a NIPT test but it is especially recommended for pregnant women:
– aged over 35 years old
– who have a personal/family history of chromosomal disorder (or from the baby’s father)
Is NIPT test risky?
NIPT test is performed by collecting blood sample which poses no threat to fetus.
What happens if the test results come back mentionng a high risk for a disorder?
We recommend you to talk to your doctor for next course of action that may include further testing.