What Is ferel echo and genetic counseling?
Non-Invasive Prenatal Testing is a highly accurate blood test that screens for common chromosomal conditions in the baby using a simple blood sample from the mother. It can be done as early as 10 weeks into pregnancy.
NIPT analyzes cell-free fetal DNA present in the mother’s bloodstream to assess the risk of:
- Down syndrome (Trisomy 21)
- Edwards syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Sex chromosome abnormalities (e.g., Turner syndrome, Klinefelter syndrome)
- Optional: Fetal sex determination (if requested)
Why Choose ferel echo and genetic counseling?
- Non-invasive – no risk of miscarriage
- Early detection – available from 10 weeks
- High accuracy – up to 99% sensitivity for common trisomies
- Safer alternative to invasive diagnostic tests like amniocentesis
- Helpful for high-risk pregnancies, IVF, or women above 35
Who Should Considerferel echo and genetic counseling?
- Women with abnormal first-trimester screening results
- Mothers age 35 and above
- Previous history of chromosomal abnormalities
- Twin or IVF pregnancies
- Those who want early and accurate reassurance
What Happens If ferel echo and genetic counseling Shows High Risk?
If your NIPT result shows an increased risk for a condition, your doctor may recommend confirmatory diagnostic tests, such as:
- Chorionic Villus Sampling (CVS)
- Amniocentesis
These tests can confirm the diagnosis before taking any medical decisions.
Why Vivid Scans?
- Trusted lab partners with validated NIPT technology
- Guided by fetal medicine consultants
- Thorough pre- and post-test counseling
- Clear result interpretation and support
Schedule Your ferel echo and genetic counseling Today
Get peace of mind with accurate, early insights into your baby’s health.
📍 Visit us at Vivid Scans, Mangadu, Chennai
📞 Call or WhatsApp for appointments: +91 95147 79997