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                                38099
BR                                38099                             US                                12911
US                                12911                             VN                                10133
VN                                10133                             AR                                3580
AR                                3580                             MX                                2801
MX                                2801                             GB                                2107
GB                                2107                             AO                                1797
AO                                1797                             CO                                1782
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