Non-invasive screening testing that reliably detects fetal genetic anomalies at the genome level from maternal blood samples.
NIPTiva Test does not pose a risk to the fetus, and it is also much more reliable than combined screening tests.
When is the ideal time for testing?
10 weeks of pregnancy is the most favorable for testing because there is a higher percentage of the baby's DNA in the mother's blood.
Risk-free for the pregnant woman and the baby!
Why NIPTiva Prenatal test?
It's safe
With a significantly more thorough approach to analysis, the accuracy of the results is as high as 99.9%
Revolutionary
The most modern and fastest version of testing on the illumine platform
Simple
Just a few steps to get the results
Fast
Results are available in just 5 to 7 working days
Safe
Non-invasive testing that poses no risk to the pregnant woman and the baby
CUSTOMER REVIEWS
Impressions of our service users
Sanja Mitrović
“In both my first and second pregnancies, I did first-trimester testing, and since the results were good in both pregnancies, there was no need for additional testing. The reason I decided to do those tests is that I wanted to know if there was a disorder in my child, so I could prepare for it.”
Vesna Dimitrijević
“I chose this type of test because it is the least invasive. I wanted the most reliable results, which I got as soon as I received the return email!”
Dragica Nikolić
“Given that I am familiar with the medical history of my family, I wanted to be sure that my eagerly awaited pregnancy was okay. We opted for the NIPTIVA test because of the simple process and the security it provides. Now I am counting down the days until I can hug my boy.”
PACKAGES
Our packages
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- X
- X
- X
- X
- X
- X
- X
- X
- X
- X
649€
/
549€
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- X
- X
- X
- X
- X
- X
- Aneuploidies of all chromosomes (1 to 22)
- Trisomies and monosomies of all chromosomes (1-22)
- Microdeletions, Deletions, Duplications of all chromosomes larger than 7Mb
- Gender information
749€
/
649€
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Aneuploidies of the sex chromosomes
- Turner syndrome (monosomy X)
- Klinefelter syndrome (trisomy XXY)
- Triple X syndrome (trisomy X)
- Jacobs syndrome (trisomy XYY)
- X
- X
- X
- X
- X
- Gender information
699€
/
599€
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Aneuploidies of the sex chromosomes
- Turner syndrome (monosomy X)
- Klinefelter syndrome (trisomy XXY)
- Triple X syndrome (trisomy X)
- Jacobs syndrome (trisomy XYY)
- X
- X
- X
- Microdeletions, Deletions, Duplications of all chromosomes larger than 7Mb
- Gender information
- X
- X
- X
- X
799€
/
699€
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Aneuploidies of the sex chromosomes
- Turner syndrome (monosomy X)
- Klinefelter syndrome (trisomy XXY)
- Triple X syndrome (trisomy X)
- Jacobs syndrome (trisomy XYY)
- Aneuploidies of all chromosomes (1 to 22)
- Trisomies and monosomies of all chromosomes (1-22)
- Microdeletions, Deletions, Duplications of all chromosomes larger than 7Mb
- Gender information
- X
- X
- X
- X
- X
899€
/
799€
- Down syndrome (trisomy 21)
- Edwards syndrome (trisomy 18)
- Patau syndrome (trisomy 13)
- Aneuploidies of the sex chromosomes
- Turner syndrome (monosomy X)
- Klinefelter syndrome (trisomy XXY)
- Triple X syndrome (trisomy X)
- Jacobs syndrome (trisomy XYY)
- Aneuploidies of all chromosomes (1 to 22)
- Trisomies and monosomies of all chromosomes (1-22)
- Microdeletions, Deletions, Duplications of all chromosomes larger than 7Mb
- Gender information
- Cystic fibrosis
- Spinal muscle atrophy
- Wilson's disease
- Gylbert syndrome
- Duchenne muscular dystrophy
1399€
/
1299€
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