Non-Invasive Prenatal Testing (NIPT)
Non-Invasive Prenatal Testing (NIPT) is an advanced and highly accurate screening test that analyzes small fragments of fetal DNA circulating in the mother’s blood. It is typically performed after 10 weeks of pregnancy and poses no risk to the baby, making it a safe and reliable option for early genetic screening.
NIPT screens for common chromosomal conditions such as:
- Down syndrome (Trisomy 21)
- Edwards syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Sex chromosome abnormalities (e.g., Turner syndrome)
Key Benefits of NIPT:
- Simple blood test with no needles or invasive procedures
- High accuracy rates (over 99% for Trisomy 21)
- Results available within 7–10 working days
- Can determine the baby’s gender, if desired
- Recommended for high-risk pregnancies or advanced maternal age
Why Choose Us?
- Certified lab partners and advanced testing technology
- Expert genetic counseling and support
- Fast, confidential, and accurate reporting
At our center, we offer Non-Invasive Prenatal Testing to give you peace of mind and early insights into your baby’s health — all without any risk to your pregnancy.
