Nuchal Translucency Scan

The Nuchal Translucency Scan, also known as the Early Anomaly Scan, is typically performed between 12 and 14 weeks of pregnancy. This safe, non-invasive scan is recommended as part of routine early pregnancy care. It is often combined with a Non-Invasive Prenatal Test (NIPT) to enhance the accuracy of first-trimester screening.

This ultrasound scan measures the fluid collection at the back of the baby’s neck, which is referred to as the “nuchal translucency.” The thickness of this fluid can provide important information about the baby’s risk for certain chromosomal conditions, such as:

1. Down syndrome (Trisomy 21)
2. Trisomy 18 (Edwards Syndrome)
3. Trisomy 13 (Patau Syndrome)
   
   

An increased amount of fluid measured during the scan may indicate a higher risk for certain chromosomal conditions, though it is not a definitive diagnosis. In such cases, further testing may be necessary. Our Consultant Fetal Medicine Specialists are available to guide you through additional testing options and advise on the next steps.

The scan will be performed in one of our specialist scanning suites at our dedicated West London clinic and take approximately 30 minutes. 

The Nuchal Translucency Scan is included in our all-inclusive Complete Pregnancy Package.