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NiptyX® by Ginekaliks laboratory
NiptyX® is a non-invasive prenatal test that detects genetic disorders, such as Down's, Edwards' and Patau's syndrome, as early as the 10th week of pregnancy. NiptyX® has the widest panel of tests - it analyzes the entire genome of the baby - all 46 chromosomes.
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Medical genetics and genomics
Ginekaliks Genetic Laboratory, a laboratory for medical genetics and genomics where we offer a wide range of services: from preconception, pregnancy, newborn and throughout childhood and adulthood - which meet the needs of our patients and maintain the quality of health services at the highest level
NiptyX® by Ginekaliks laboratory
Overview of NiptyX®
NiptyX® is a non-invasive prenatal screening test (or cell-free DNA screening) for pregnant women to assess the risk that the fetus will be born with certain chromosomal abnormalities. NiptyX® is available for singleton, twin and egg donor pregancies. Well-trusted globally, NiptyX® can assess conditions that may affect your baby's health by doing a simple blood draw on you. NiptyX® screens for common chromosomal abnormalities, including trisomies, sex chromosome aneuploidies, and microdeletion/duplication syndromes, and can provide information about the sex of your babies.
NiptyX® by Ginekaliks laboratory
Why choose NiptyX®?
Reilable
More than 10 million pregnant women worldwide have taken the NiptyX® test so far, with the lowest false positive rate of 0.14%. Highest success rate of 99.902%
Safe & Fast
No risk for the baby and the laboring woman. Already from the 10th week of pregnancy, by analyzing a standard sample of 10 ml of maternal venous blood. Also suitable for twins, VTO and pregnancies with a donated egg. Result in 6-10 days.
Complete
NiptyX® and NiptyX® Pro tests analyze all 46 chromosomes of the baby. Broadest panel of tests: all trisomies (1-22), sex chromosome aneuploidies (X,Y), deletion/duplication syndromes (60 larger than 5Mb in the Plus package; 84 larger than 3Mb in the Pro package), incidental findings with clinical interpretation.
Precise
The rate of proven trisomy detection is greater than 99% and confirmed by the largest NiptyX® clinical trial in the world on almost 147,000 pregnancies.
NiptyX® by Ginekaliks laboratory
How NiptyX® test works?
During pregnancy, fetal DNA enters into maternal bloodstream. Next-generation technology makes it possible to analyze free fetal DNA segments that are present in maternal blood in order to identify chromosomal abnormalities. NiptyX® test requires only 10 ml maternal blood sample and blood collection can be performed during the 10th pregnancy week.
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NiptyX® by Ginekaliks laboratory
NiptyX® Workflow
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Order Your Prenatal Test Kit
Start by ordering our specialized prenatal test kit from our website. Designed for expectant mothers, this kit includes everything needed for a safe and easy blood sample collection
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Visit a Local Lab for Sample Collection
Take the test kit to any local laboratory. A trained healthcare professional will assist you in gently collecting a small blood sample. This process is quick and designed to ensure both your comfort and the reliability of the test
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Send Us the Blood Sample
Once your sample is collected, securely place it in the provided test tube and use the pre-addressed, postage-paid packaging to mail it back to our laboratory. We handle your sample with the utmost care and precision.
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Receive Comprehensive Prenatal Results
Our sophisticated lab will analyze your sample for a comprehensive prenatal diagnosis. We'll provide you with a detailed report that offers insights into your baby's health and development. You'll receive these results quickly and securely, enabling you to make informed decisions about your pregnancy
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