Non-invasive prenatal screening (NIPT)
Panorama™ NIPT
A single blood draw from the mother is enough for Panorama™ to screen the baby’s DNA for the most common chromosomal conditions. Choose the panel that suits you, send your order and our team will contact you to confirm the details and the blood draw appointment.
- SampleOne maternal blood draw
- WhenFrom week 9 of pregnancy
- Results10 working days
Choose your panel
All panels are performed from the same blood sample. Your doctor can help you choose the right one.
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Panorama Plus
Screening for the most common chromosomal conditions and 22q11.2 deletion syndrome (DiGeorge syndrome).
- Trisomy 21 (Down syndrome)
- Trisomy 13 (Patau syndrome)
- Trisomy 18 (Edwards syndrome)
- Triploidy
- Sex chromosome abnormalities
- Monosomy X
- 22q11.2 deletion syndrome (DiGeorge syndrome)
- Fetal sex (optional)
Price on request
Order this panel -
Panorama Full
The most comprehensive option: everything in Panorama Plus, plus four more microdeletion syndromes.
- Everything in Panorama Plus
- 1p36 deletion syndrome
- Cri-du-chat syndrome
- Angelman syndrome
- Prader-Willi syndrome
Price on request
Order this panel
Panel availability depends on the type of pregnancy (for example twins or egg donor pregnancies). Microdeletion screening is optional; its performance is more limited than for trisomies.
Order Panorama™
Fill in the form and our team will contact you as soon as possible to complete your order.
No payment is taken at this step. Our team confirms the price and the payment method with you before the blood draw.
Have a question first? See our frequently asked questions.