Non-invasive prenatal screening for common chromosomal conditions, including trisomy 21, 18, and 13, with sex chromosome screening and fetal sex reporting.
Available from 10 weeks of pregnancy, this simple blood test provides important early insights into your pregnancy.
- Trisomy 21 (Down syndrome)
- Trisomy 18 (Edwards syndrome)
- Trisomy 13 (Patau syndrome)
- Monosomy X (Turner syndrome)
- XXX (Triple X syndrome)
- XXY (Klinefelter syndrome)
- XYY (Jacobs syndrome)
- Fetal sex reporting
- Twin pregnancy screening*
* For twin pregnancies, only Y chromosome detection is available.
