Early Screening, Lifelong Peace of Mind
Pregnancy care should be rooted in safety, accuracy, and empathy. CareWell Diagnostix is equipped with state-of-the-art tools to perform prenatal NT scans for Down Syndrome detection, ensuring your care is both clinically sound and emotionally supportive.
How Down Syndrome Screening is Performed?
Here is the process in brief:
First Trimester Screening (11-14 weeks)
Plasma protein-A (PAPP-A), nuchal translucency (NT), and human chorionic gonadotropin (hCG) test.
Combined Test (11-14 weeks)
Blood test and NT ultrasound with maternal age to assess the risk of Down syndrome.
Quadruple Test (15-20 weeks)
Alpha-fetoprotein (AFP), unconjugated estriol (uE3), hCG, and inhibin A blood tests.
Anomaly Scan (18-20 weeks)
Detailed ultrasound to assess foetal anatomy, increased nuchal fold thickness, absent nasal bone, and echogenic bowel.
Cell-Free DNA Test (cfDNA) (after 10 weeks)
Chromosomal abnormalities test
Evidence-Based Care, Delivered with Empathy
For complete assurance during pregnancy, expert diagnostics are essential. CareWell Diagnostix brings together compassionate care and leading technology to support your journey through all required screenings.
Plan Ahead. Stay Informed. Stay Safe.
Preparing for your prenatal test begins with awareness. Knowing what to expect ensures your journey through pregnancy is smooth, safe, and stress-free. Our team at CareWell Diagnostix is here to guide you every step of the way.
Contact us today!
