NICC® is a simple, safe and accurate non-invasive prenatal test (NIPT) to screen for common chromosomal abnormalities as early as 10 weeks of pregnancy.
American College of Medical Genetics and Genomics
Peace of Mind
NICC® provides complimentary post-test genetic counselling for high risk cases
99% accuracy for the detection of Down Syndrome, Edwards Syndrome and Patau Syndrome
NICC® is non-invasive, there is no risk of miscarriages
NICC® is covered by insurance and provides complimentary diagnostic test for high risk cases
|NICC® Screens for|
Down Syndrome (Trisomy 21)
Edwards Syndrome (Trisomy 18)
DiGeorge Syndrome 2
Van der Woude Syndrome
Sex Chromosome Aneuploidies:
Turner Syndrome (XO)
Klinefelter Syndrome (XXY)
Triple-X Syndrome (XXX)
Jacob's Syndrome (XYY)
During pregnancy, cell-free fetal DNA (cffDNA) is released from placenta into the mother’s blood vessel.
Using only 10 ml of the mother’s blood, NICC® detects the baby’s DNA and measures the risk of chromosomal abnormalities using Next-Generation Sequencing (NGS) method.
Find out more about other prenatal tests:
- First Trimester Screening
- Second Trimester Screening
- Pre-Eclampsia Screening
- CC (ChromosomesCheckTM)
- Karyotype Anlysis
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