NIFTY® Twin
by Ginekalikslab
Unlike traditional prenatal screenings, the NIFTY® Twin test uses a simple blood sample from the mother to analyze the twins; DNA, providing results with over 99% accuracy. This means parents can receive critical health information about their babies very early, allowing for timely medical advice and peace of mind throughout pregnancy.
NIFTY® by Ginekalikslab
Overview of NIFTY® Twin
The NIFTY® Twin test is a specialized version of the NIFTY® series of non-invasive prenatal tests (NIPT), designed specifically for pregnancies involving twins. Twin pregnancies present unique challenges in prenatal screening, and the NIFTY® Twin test is developed to address these challenges, providing accurate and comprehensive screening for chromosomal abnormalities like the Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome) and Trisomy 13 (Patau syndrome) in twin pregnancies.
NIFTY® by Ginekalikslab
Why choose NIFTY® Twin?
Early Detection: The NIFTY® Twin test can provide early detection of chromosomal abnormalities, which is crucial in twin pregnancies where managing potential complications can be more challenging.
Specialized for Twins: The test is specifically designed for twin pregnancies, offering more accurate results than the traditional prenatal screenings, which may not account for the complexities of analyzing DNA from two fetuses.
Non-Invasive and Safe: Like other NIPT tests, the NIFTY® Twin test is non-invasive and requires only a blood sample from the mother, posing no risk to the fetuses.
Peace of Mind and Informed Decision-Making: The NIFTY® Twin test can provide peace of mind by either ruling out common chromosomal abnormalities or allowing you to prepare for a child with special needs.
Personalized Care: If the test indicates a high risk of chromosomal abnormalities, it allows for more personalized and proactive prenatal care, including the possibility of further diagnostic testing.
Accuracy and Reliability: higher then 99%
NIFTY® by Ginekalikslab
How NIFTY® 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. NIFTY® test requires only 10 ml maternal blood sample and blood collection can be performed during the 10th pregnancy week.
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NIFTY® by Ginekalikslab
NIFTY® Twin Workflow
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Pre-Test Counseling: Call our laboratory to consult with our geneticists free of charge and find all the answers to your questions so you can choose the best option for your baby.
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Order your prenatal test kit: Start by ordering our specialized prenatal test kit from our website. This is supported by a global leader in the logistics industry. Designed for expectant mothers, this kit includes everything needed to safely and easily collect a blood sample.
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Visit a local laboratory for sample collection: Take the test kit to any local laboratory. A trained healthcare professional will help you gently collect a small 10ml blood sample. This process is non-invasive and 100% safe for yourself and your baby. It is quick and designed to ensure both your test convenience and confidentiality.
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Send us a blood sample: Once your blood sample is collected, place it securely in the box provided and use the pre-addressed, postage-paid packaging to send it back to our laboratory.
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Laboratory Analysis: Our sophisticated laboratory will analyze your sample for a comprehensive prenatal diagnosis. The fetal DNA is being isolated from the mother’s blood and is being tested with the advanced NGS technology (CNV > 3 Mb) across the whole genome with a 99% accuracy.
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Reporting and interpretation: We will inform you on the phone and provide you via email with a detailed report that offers information for Trisomy 21, 18, 13 (+ incidental findings) related to your baby's health and development. You will receive these results in 7 – 10 days quickly and safely, while having the chance to discuss the results with our specialized team and geneticists. They will help you understand your results and make sure you receive all the information, any time, 24/7 at your disposal.
Why NIFTY®?
Why you should choose NIFTY®
NIFTY® (Non-Invasive Fetal Trisomy) | First Trimester Screening | Quad Screen | |
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Timing of Test | After 9 weeks of pregnancy | 11-14 weeks of pregnancy | 15-20 weeks of pregnancy |
Detection Rate for Trisomy 21 | ~99% | ~85-90% | ~80-85% |
Detection Rate for Trisomy 18 | ~97% | ~80% | ~70-80% |
Detection Rate for Trisomy 13 | ~95% | ~70% | ~60-70% |
False Positive Rate | ~0.1% | ~5% | ~5% |
Invasive Testing Required | No | No | No |
Risk of Miscarriage | None | None | None |
Accuracy | Very High (based on analysis of fetal DNA) | Moderate (based on a combination of blood markers and ultrasound) | Moderate (based on multiple serum markers) |
Follow-Up Testing | If high risk is indicated, diagnostic tests (e.g., amniocentesis or CVS) | If high risk is indicated, diagnostic tests | If high risk is indicated, diagnostic tests |
Test Procedure | Simple blood draw from mother | Blood test and ultrasound combined | Blood test from mother |
Turnaround Time for Results | Typically 1-2 weeks | Typically 1-2 weeks | Typically 1-2 weeks |
Impact on Pregnancy Management | Helps inform about risk, can lead to more targeted diagnostic testing | Helps assess risk but might lead to further testing | Helps assess risk but might lead to further testing |