Nuchal Translucency Screening
Nuchal Translucency (NT) Screening is a specialized ultrasound scan performed between 11 and 14 weeks of pregnancy. It measures the fluid-filled space at the back of the baby’s neck — an important indicator of certain chromosomal conditions and genetic disorders.
This non-invasive screening helps assess the risk of:
- Down syndrome (Trisomy 21)
- Edwards syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Certain heart defects and developmental issues
At our center, we perform NT screening using high-resolution ultrasound technology under the guidance of skilled and certified sonologists. The scan is quick, painless, and completely safe for both mother and baby. For more accurate results, it is often combined with a blood test as part of the first-trimester combined screening.
Why Choose Us?
- Advanced imaging systems
- Experienced fetal medicine specialists
- Detailed and timely reporting
- Supportive counseling based on findings
Early screening empowers you with information and helps your doctor plan the next steps in care if needed. With Nuchal Translucency Screening, we help you begin your pregnancy journey with clarity, confidence, and expert guidance.
