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In every 775 births
Ensuring early detection and peace of mind through cutting-edge prenatal screening technology.
Need help choosing a test?
Talk to our team of experts to help you choose which test is best for you.
Basic Test
The following common chromosomal abnormalities will be screened: Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards' Syndrome), Trisomy 13 (Patau Syndrome), and gender identification if you choose to know.
4 Condition Tests
NIPT Basic provides tests for 4 conditions
What's Included?
4 Tests
Early Detection
Identifies issues early in pregnancy for proactive care.
Accurate results
Over 99% accuracy in detecting chromosomal conditions.
Non-Invasive
Safely conducted using a simple blood sample from the mother.
Gender Reveal
Discovers your baby's gender during the testing process.
Avail affordable pricing and attractive discounts or cash backs on each purchase.
When you choose to check out with Tabby in 4 monthly installments.
For easier understanding and health monitoring.
For same day testing or schedule easily for next day and beyond.
They will guide you live over video and answer all of your questions.
For processing your samples with industry leading accuracy.
When you book using the DarDoc app.
You may have seen us in the news lately. It's all the chatter about how we are changing the game.
NIPT screens for common chromosomal abnormalities such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13). Some tests may also screen for additional conditions like sex chromosome aneuploidies and microdeletions.
NIPT is highly accurate, typically achieving over 99% accuracy in detecting the screened conditions. However, it's important to note that NIPT is a screening test and not diagnostic. Confirmatory diagnostic testing may be recommended for positive results.
NIPT can usually be performed as early as 10 weeks into pregnancy. It's important to consult with your healthcare provider to determine the best time based on your individual circumstances.
Yes, NIPT is considered safe for both the mother and the baby. It is a non-invasive test that requires only a blood sample from the mother, posing no known risks of miscarriage or harm to the pregnancy. It is a recommended option for prenatal screening.
