EARLY
RELIABLE
INNOVATIVE






SAFE
COMPREHENSIVE
SECURE
What does NIPTIFY provides?

Five most common chromosomal diseases
- Down syndrome
- DiGeorge syndrome (microdeletion)
- Edwards syndrome
- Turner syndrome
- Patau syndrome

Seven clinically relevant microdeletions
- Williams-Beuren syndrome
- 1p36 deletion syndrome
- Angelman and Prader-Willi syndrome
- Wolf-Hirschhorn syndrome
- Jacobsen syndrome
- Cri-du-chat or cat-cry syndrome
- Langer-Giedion syndrome

A large set of other conditions
- Trisomy 16 and trisomy 22
- Klinefelter syndrome (XXY)
- Jacobs syndrome (XYY)
- Triple X syndrome (XXX)

Fetal sex

Choose the most suitable clinic for you to make an appointment with your obstetrician or midwife and perform the NIPTIFY test.
The accuracy and broad scope of the NIPTIFY leave only one puzzle for future parents - “What name should we pick for our baby?“

Kaarel Krjutškov, PhD
CEO, Principal Inventor of NIPTIFYWhy should you choose NIPTIFY for microdeletion detection?
Why should you choose NIPTIFY for microdeletion detection?

NIPTIFY is a CE-IVD-validated and registered in vitro medical diagnostic device. The test can be distributed all over European Union.

The NIPTIFY medical laboratory has ISO 15189:2012 accreditation and follows the highest standards.

NIPTIFY participates in the EMQN quality assurance test and has consistently earned the highest possible scores.
TECHNOLOGY
NIPTIFY uses the modern Focus Plus DNA sequencing technology, which enriches fetal DNA. As a result, NIPTIFY analysis 3.6 times more fetal origin DNA than a regular NIPT test, increasing the accuracy and sensitivity.
Focus Plus technology is designed for routine and reliable screening purposes. The need for re-testing is close to zero, and the test is suitable for overweight patients.