Description
Sample Collection is conducted at home by Licensed nurses. The collected samples are sent to Licensed and accredited laboratories for reporting.
Parameters Included:
Common Autosomal Trisomies
- Chromosome 21 (Down syndrome)
- Chromosome 18 (Edwards syndrome)
- Chromosome 13 (Patau syndrome)
- Gonosomal chromosomes
- Fetal gender
Sex Chromosome Aneuploidies*
- XO (Turner syndrome)
- XXY (Klinefelter syndrome)
- XXX (Triple-X syndrome)
Incidental findings*
- Other autosomal aneuploidies
Sex Indication*
- Y chromosome detection
Advantages
- Accurate: Over 99% sensitivity for trisomy 21, 18, and 13
- Safe: Only maternal peripheral blood is needed, no risk to mother or fetus.
- Trusted: Over 15,000,000 samples processed worldwide.
- Early: Screen as early as the 10th week of pregnancy.
The test is suitable for
- Any age of pregnant women from 10 weeks gestation
- Singleton, twins, and vanishing twin syndrome (VTS) pregnancies
- IVF pregnancies
