Basic NICC Test
What’s Inside This Prenatal Screening
-
Blood Test:
Screens for common chromosomal conditions —
• Trisomy 21 (Down Syndrome)
• Trisomy 18 (Edwards Syndrome)
• Trisomy 13 (Patau Syndrome) -
Ultrasound (Nuchal Translucency Scan):
Measures the fluid behind your baby’s neck to assess the risk of chromosomal abnormalities. -
Doctor Consultation:
Review results and receive tailored advice from our caring doctors.
Why It’s a Must for You
Perfect for expectant mothers between 11 and 13 weeks of pregnancy, this package combines blood testing and ultrasound to detect the most common chromosomal abnormalities early, safely, and accurately.
BR 29800 
VN 13340 
US 4402 
AR 2924 
MY 2008 
CN 1475 
EC 1350 
IN 976 
