Get an NT (Nuchal Translucency) scan at VRX Diagno Lounge, Goregaon West — done between 11–14 weeks of pregnancy to screen for chromosomal abnormalities (Down syndrome and others), confirm gestational age, and identify some major structural defects early. Same-day radiologist-reviewed report.
The Nuchal Translucency (NT) Scan is a first-trimester ultrasound performed between 11 weeks 0 days and 13 weeks 6 days. It measures the fluid-filled space at the back of the foetal neck — increased thickness raises the risk of Down syndrome (trisomy 21), trisomy 18, trisomy 13, and major heart defects. Combined with maternal serum markers (Double Marker — PAPP-A and free βhCG), it gives a combined first-trimester risk.
Increased NT (above 3 mm) raises trisomy 21 risk significantly
Severely raised NT also increases risk for these aneuploidies
Increased NT correlates with foetal heart defects independently of chromosomes
Crown-rump length confirms gestational age
Identifies twins and chorionicity (mono/dichorionic)
Detects some major structural abnormalities (anencephaly, abdominal wall defects)
Recommended as part of first-trimester screening
Higher baseline aneuploidy risk
In previous pregnancy or family
NT is a useful early cardiac screen
Routine in assisted-conception pregnancies
Higher anomaly risk — early screening important
Always pair with Double Marker for highest accuracy
Reassurance scan with high detection rate
| Parameter | What It Measures | Reference Range |
|---|---|---|
| NT Measurement | Fluid behind foetal neck | < 3.0 mm (typical) |
| Increased NT | Raised aneuploidy / cardiac risk | > 3.0 mm |
| CRL | Crown-rump length | 45–84 mm (valid window) |
| Nasal Bone | Marker — present / absent | Present (normal) |
| Combined Risk | NT + maternal age + Double Marker | Reported with cut-off |
| Markers Reviewed | Anatomy survey, viability, dates | All documented |
NT under 3 mm with normal Double Marker and good first-trimester anatomy gives a low combined risk. Continue routine yearly screening if you have risk factors.
Increased NT (above 3 mm) or high combined risk warrants genetic counselling and consideration of NIPT, CVS, or amniocentesis for definitive diagnosis. Your physician will correlate with symptoms and history.
Every report is reviewed by an experienced pathologist with clear interpretation and clinical comment.
If further evaluation is needed — Double Marker, NIPT (cell-free DNA), Chorionic Villus Sampling, Amniocentesis, Foetal Echo, Genetic Counselling — all available at the Goregaon West centre.
Our Goregaon West centre is on S V Road, easily accessible by train, bus, and auto from all parts of the western suburbs. We provide NT Scan and other imaging services to patients from the following nearby areas:
Performed at our Goregaon West centre by qualified radiology team. Pre-book to skip the queue — same-day report.
Visit any of our 3 centres for NT Scan and other diagnostic services — walk-ins welcome
Practical answers about preparation, ranges, and booking