Description
A prenatal test that screens for common chromosomal abnormalities such as trisomies 21 (Down syndrome), 18 (Edwards syndrome), and 13 (Patau syndrome). It uses next-generation sequencing to analyze fetal DNA fragments present in the mother's blood, offering a safe alternative to invasive procedures like amniocentesis.
This lab test includes home sample collection via a provided kit or by a clinician, and you'll receive a comprehensive physical health report with your results.