Our NIPT service provides a safe, reliable, and stress-free way to gain early insights into your baby’s health from as early as 10 weeks.
Using a simple blood test combined with an ultrasound scan, we can screen for common chromosomal conditions with over 99% accuracy. This advanced NIPT test helps you feel more informed and prepared as you plan for your baby’s arrival.
The NIPT works by analysing fragments of your baby’s DNA (cell-free DNA) in your bloodstream. These fragments come from both maternal and placental cells, allowing us to identify the risk of certain chromosomal conditions:
● Trisomy 21 (Down’s syndrome)
● Trisomy 18 (Edwards’ syndrome)
● Trisomy 13 (Patau’s syndrome)
If requested, we can also determine fetal sex, providing even greater insight. Your results will be ready within 3-5 working days and will be communicated directly by our qualified midwife sonographer.