What is NIPT Test ( Fetal DNA Test )?
What is NIPT Test ( Fetal DNA Test )?Non – Invasive Prenatal Diagnosis (NIPT Test)
NIPT (Non-Invasive Fetal Trisomy Test) is a safe and rapid non-invasive prenatal test that offers the opportunity to screen for certain genetic conditions starting from the 10th week of pregnancy.
Using the most advanced genetic sequencing technology, NIFTY has a 99% success rate in detecting the three most common trisomy conditions at birth, Down syndrome, Edwards syndrome and Patau syndrome.
NIFTY Test ( Fetal DNA Test ) has been applied to 146,958 pregnant women starting from the 10th week of pregnancy, with the opportunity to test with 10 ml of blood taken from the mother, without intervention and without the risk of miscarriage. It is the test with the highest clinical validation with more than one test.
The NIFTY test ( Fetal DNA Test ) is a non-invasive prenatal test (often called NIPT) that screens for Down syndrome and other specific genetic conditions that result from excess or missing genetic information in baby DNA. NIFTY involves drawing a small amount of blood from the mother and can be done from week 10. Results are available within 10 working days. Fetal DNA (NIFTY) has a higher success rate than traditional screening methods and does not pose a miscarriage risk to the mother or baby, unlike invasive (interventional) procedures such as amniocentesis.
- Trisomys Sex Chromosome Aneuploidies Deletion Syndromes
- Down Syndrome Turner Syndrome Cri-du-chat
- Edwards Syndrome Klinefelter Syndrome 1p36
- Patau Syndrome Triple -X 2q33.1
- Trisomy 22 XYY Karyotype Prader-Willi / Angelman Syndrome (15q11.2)
- Trisomy 16 Jacobsen Syndrome (11q23)
- Trisomy 9 DiGeorge Syndrome II (10p14-p13)
- 16p12
- Van der Woude Syndrome (1q32.2)
Testing services for trisomy conditions are suitable for twin pregnancy, surrogacy and IVF conditions.
NIPT Test
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