NIPTIFY – single pregnancy chromosomal screening
NIPTIFY (Non-Invasive Prenatal Test) is a modern and reliable method for the early detection of fetal chromosome conditions, such as Down, Edwards, and Patau syndromes, as well as sex chromosome abnormalities. This test is performed from the 10th week of pregnancy using a sample of the mother’s venous blood, making it completely safe for the baby. NIPTIFY offers significantly higher accuracy than standard screening tests and helps expectant parents make informed decisions about the course of their pregnancy.
When to see a specialist
- Down syndrome (Trisomy 21): Detection of the most common fetal chromosome condition.
- Edwards syndrome (Trisomy 18): Detection of a severe chromosome condition.
- Patau syndrome (Trisomy 13): Detection of a severe chromosome condition.
- Sex chromosome abnormalities: Detection of syndromes such as Turner (X0), Klinefelter (XXY), Triple X (XXX), and XYY.
- Increased risk of chromosome abnormalities: If previous screening tests (e.g., the OSCAR test) have shown an increased risk.
- Maternal age: The risk of chromosome abnormalities increases if the mother is over 35.
- Desire to avoid invasive tests: NIPTIFY is a safe alternative to invasive procedures (e.g., amniocentesis or chorionic villus sampling).
- Desire for early and accurate information: The test provides a reliable result early in the pregnancy.
Common symptoms
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You are over 35 years old
The risk of chromosome abnormalities increases with age. -
You are pregnant and want accurate information about your baby’s chromosomes
NIPTIFY is recommended for all pregnant women who want extra reassurance. -
You have a family history of chromosome conditions
If there have been chromosome abnormalities in your family. -
You want to avoid invasive tests
NIPTIFY is a safe and non-invasive alternative. -
Your previous screening tests have shown an increased risk
NIPTIFY helps to clarify this risk.
How to prepare for your appointment
- The test can be performed from the 10th week of pregnancy onwards.
- Bring your ID card or another form of identification.
- Think about any questions you may have about the test and ask our staff before the procedure.
What to expect during your appointment
Consultation
We will ask you detailed questions about your health, medical history, and pregnancy. We will explain the NIPTIFY test, its benefits, limitations, and possible results.
Blood sample collection
We will take a sample of your venous blood. This is a quick and painless procedure.
Sample analysis
Your blood sample is sent to a laboratory for analysis, where the baby’s DNA is isolated and analyzed for chromosome abnormalities.
Waiting for results
We usually receive the results within 10 working days.
Receiving results and counseling
We will give you the test results and explain what they mean. If the test result is positive, we offer further counseling and, if necessary, refer you for invasive diagnostic tests (e.g., amniocentesis or chorionic villus sampling) to confirm the diagnosis.
Specialists providing this service
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dr Jaanika Heinväli
resident gynecologist
Rävala Clinic – Specialist Medical Care and Occupational Health
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Payment & Appointment Info
Prices
Tallinn
| Service | Price |
|---|---|
| Visit fee Added to the appointment fee. | 20 € |
| NIPTIFY prenatal chromosome test The specialist consultation fee and visit fee will be added to the price. | 315 € A visit fee is added to the price. |
Everywhere else in Estonia
| Service | Price |
|---|---|
| Visit fee Added to the appointment fee. | 13 € |
| NIPTIFY prenatal chromosome test The specialist consultation fee and visit fee will be added to the price. | 315 € A visit fee is added to the price. |
Payment methods
This service is not covered by Meliva Health Insurance. Check your personal coverage limits in the ERGO app.
Referral
You can book this service as a self-paying patient without a doctor’s referral.
Who is this appointment for?
NIPTIFY is for women with singleton pregnancies from the 10th week of pregnancy.
The test is a screening test, not a diagnostic test. A positive result always requires confirmation with invasive methods.
The test does not detect all chromosome abnormalities or other birth defects.
The accuracy of the test is very high, but not 100%.
For multiple pregnancies (twins, triplets), interpreting the NIPTIFY test is more complex, and you should consult with a doctor about its suitability.
Clinics offering this service
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Open
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Open
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Frequently Asked Questions
What is NIPTIFY?
NIPTIFY is a non-invasive prenatal test that analyzes the baby’s DNA from the mother’s blood to detect the most common chromosome abnormalities, such as Down, Edwards, and Patau syndromes.
When can the NIPTIFY test be done?
The NIPTIFY test can be done from the 10th week of pregnancy.
Is NIPTIFY safe for the baby?
Yes, NIPTIFY is completely safe for the baby, as it only requires a sample of the mother’s venous blood.
What does the NIPTIFY test show?
The NIPTIFY test shows the risk for Down, Edwards, and Patau syndromes, as well as sex chromosome abnormalities. If desired, the baby’s sex can also be determined.
Do I need a referral for the NIPTIFY test?
No, a referral is not needed for the NIPTIFY test.
How accurate is the NIPTIFY test?
The NIPTIFY test is very accurate, with a detection rate of over 99% for the most common chromosome abnormalities.