Why choose PrenatalSafe NIPT?
- Early Detection: Available from 10 weeks of pregnancy, allowing for early reassurance.
- High Accuracy: Detects over 99% of cases of Down’s syndrome (Trisomy 21), with similarly high detection rates for Edwards syndrome (Trisomy 18) and Patau syndrome (Trisomy 13).
- Safe and Simple: Requires only a single tube of maternal blood; no risk to you or your baby.
- Quick Results: Results are typically available within 2–5 working days.
- Low Failure Rate: Less than 0.5% of tests fail to produce a result, reducing the need for repeat testing.
- Optional Gender Reveal: Find out your baby’s sex with over 99% accuracy, if you wish.
What conditions does PrenatalSafe screen for?
- Down’s Syndrome (Trisomy 21): A genetic condition causing learning disabilities and characteristic physical features.
- Edwards Syndrome (Trisomy 18): Associated with severe developmental delays and physical abnormalities.
- Patau Syndrome (Trisomy 13): Linked to serious intellectual disability and physical defects.
- Optional Fetal Sex Determination: Know your baby’s sex early, if desired.
How does the test work?
During pregnancy, small fragments of your baby’s DNA circulate in your bloodstream. PrenatalSafe NIPT analyses this cell-free DNA using advanced whole-genome sequencing technology to detect chromosomal abnormalities. The test is non-invasive and poses no risk to you or your baby.
Who Should Consider PrenatalSafe NIPT?
PrenatalSafe NIPT is suitable for all pregnant women, regardless of age or risk factors. It is especially recommended if:
- You want early and accurate information about your baby’s health.
- You have a higher risk of chromosomal conditions due to age or family history.
- You prefer to avoid invasive diagnostic tests like amniocentesis.




























