Purpose of the Procedure
- Early screening for Down Syndrome (Trisomy 21) risk.
- Identifying risks for other chromosomal conditions like Edwards Syndrome.
- Confirming healthy fetal development in the early stages.
A precise first-trimester ultrasound assessing fetal neck thickness to screen for potential chromosomal abnormalities, providing essential early insights and peace of mind during your pregnancy journey.
Scientific name: First Trimester Nuchal Translucency Scan (NT)
A specialized ultrasound performed between weeks 11 and 13 to measure the fluid-filled space behind the fetal neck, serving as a primary screening tool for chromosomal aneuploidies.