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.
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Malaysia
