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                                32172
BR                                32172                             VN                                11069
VN                                11069                             US                                6670
US                                6670                             AR                                3056
AR                                3056                             EC                                1438
EC                                1438                             CN                                1410
CN                                1410                             MY                                955
MY                                955                             BD                                917
BD                                917                             
         
        
 
        