Cell-free fetal DNA analysis
From around 10 weeks, fragments of placental DNA circulate in maternal blood. NIPT analyses this material to detect chromosomal abnormalities. Detection rates exceed 99 percent for Down syndrome with very low false positive rates.
Standard NIPT panel
Standard NIPT screens for trisomies 21, 18, 13 and sex chromosome conditions (Turner, Klinefelter, XYY, XXX). Expanded panels test for additional microdeletions but with progressively reducing positive predictive value.
What NIPT does not do
- Screens chromosomal conditions only – does not detect structural anomalies
- Is a screening test, not diagnostic – positive results need CVS or amniocentesis confirmation
- Can be inconclusive in cases of low fetal fraction
- Does not replace ultrasound scanning for structural assessment
Your fetal-medicine specialist
Your screening pathway is led by a clinician dedicated to fetal medicine, with a direct pathway to senior gynaecologist Dr. Priyadatt Patel for any pregnancy that needs obstetric care.
Dr. Mayank Chaudhary
An ISUOG-trained fetal-medicine consultant who guides NIPT and screening choices and explains results clearly so you can decide with confidence.
Standards & further reading. Our approach aligns with the NHS antenatal screening and the ISUOG guidelines.
Related fetal-medicine pages
NT ScanAnomaly Scan (TIFFA)Doppler ScanPrenatal GeneticsAmniocentesisCVSCVS vs AmniocentesisFetal MedicinePregnancy Care
Frequently asked
Dr. Priyadatt Patel
Senior Gynecologist · Advanced Laparoscopic Surgeon · IVF and Endometriosis Programme Lead
MS OBGyn · Pregnancy Care · Advanced Gynaecological Ultrasound · Fertility Preservation
ESHRE / ESGE / AAGL / ASRM guideline-aligned practice. 3D Karl Storz precision technique. Fertility-preservation-first philosophy. Evidence-based decisions, honest counselling, long-term outcomes orientation.
Science City Road, Ahmedabad 380060
Mon–Sat 11:00–20:00 · +91 97234 31544
Naranpura, Ahmedabad
Mon–Sat 08:30–10:30 · +91 70460 02566
