NIPT
What is NIPT?
NIPT ( Non-Invasive Prenatal Testing) is a simple blood test which can be taken from around 10 weeks into pregnancy. It can screen for the most common chromosomal conditions like Down syndrome, Edwards syndrome and Patau syndrome.
Our tests can also look at the 22 chromosomal pairs, six syndromes caused by the absence of a small portion of specific chromosomes (microdeletion) and sex chromosomes. Please see the chart below for more information on what can be screened for.
How does it work?
By analyzing cell-free DNA (cfDNA) from the placenta that circulates in the mother’s blood. There is no risk of miscarriage.
Is NIPT available on the NHS?
NIPT is only available on the NHS for people who have had their 12-13 week scan and had a high risk result, or have history of a pregnancy with a previous chromosomal abnormality. The NHS NIPT only screens for Downs, Edwards and Patau’s syndromes.
Why should I choose Discovery Ultrasound for my NIPT?
We have specially chosen laboratories that give excellent, consistent results. We use Future Health Biobank, we can also offer the Panorama test – we are the only clinic in Sussex and Kent to offer this test.
We are able to arrange an appointment with genetic counsellors to talk to you in detail about your results. We also have close links with our NHS trust and will refer you quickly in the event of a high chance result.
We will inform you when to expect your results and we will call you in addition to sending you the results to ensure you have the opportunity to ask questions.
We understand that choosing the right test can feel a little confusing. Please feel free to call us or send us message and we can talk about all the options.
All our NIPTs include a scan at same time. This can be done before your NHS first trimester scan or after. We will always do our very best to look after you at all stages, because we care!
How accurate is NIPT?
It offers a high detection rate and a very low false positive rate for common chromosomal abnormalities.
The latest clinical performance for Future Health Biobank test;
https://yourgenehealth.com/our-products/nipt-solutions/nipt/iona-nx#pac_dtm_child_2
| | FHL NIPT | FHL NIPT+ | FHL NIPT+ with microdeletions | Panorama | Panorama Extended |
|---|---|---|---|---|---|
| Price with scan | £380 | £430 | £615 | £380 | £530 |
| Available from | 10 Weeks | 10 Weeks | 10 Weeks | 9 Weeks | 9 Weeks |
| T13, T18 & T21 (Down’s, Edwards’ & Patau’s) | Yes | Yes | Yes | Yes | Yes |
| Sex chromosome aneuploidy | Yes | Yes | Yes | Yes | Yes |
| Fetal sex (optional) | Yes | Yes | Yes | Yes | Yes |
| All chromosomal pairs 1-22 | No | Yes | Yes | No | No |
| Triploidy | No | No | No | Yes | Yes |
| Microdeletion Syndromes | None | None | DiGeorge syndrome, 1p36 deletion syndrome, Angelman syndrome, Prader-Willi syndrome, Cri du Chat syndrome, Wolf-Hirschhorn syndrome | None | DiGeorge syndrome, 1p36 deletion syndrome, Angelman syndrome, Prader-Willi syndrome, Cri du Chat syndrome |
| Laboratory | Future Health Laboratories, UK | Future Health Laboratories, UK | Future Health Laboratories, UK | Natera, USA | Natera, USA |
| Genetic counselling included | Yes | Yes | Yes | Yes | Yes |
| Lab accreditation | Yes | Yes | Yes | Yes | Yes |
| Results turnaround time from arrival at lab | 5-7 working days | 5-7 working days | 5-7 working days | 7-10 working days | 7-10 working days |
- Trisomy 21 (Down syndrome)
- Trisomy 18 (Edwards syndrome)
- Trisomy 13 (Patau’s syndrome)
- Sex Chromosome Aneuploidies (SCAs)
- Certain microdeletions
Book an appointment
Please give us a call on 01424 230297 to book your NIPT scan