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NICC NICC Pregnancy Health

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
(ACMG), recommends:


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

What does NICC® screen for?

The risk of having a child with chromosomal abnormalities, such as Down Syndrome (Trisomy 21), Edwards Syndrome (Trisomy 18) and Patau Syndrome (Trisomy 13) increases with maternal age. Diagnostic tests for trisomy detection such as amniocentesis and chorionic villus sampling (CVS) are invasive and impose a risk of miscarriage to the pregnancy. NICC® is a highly accurate screening test that provides a stronger risk indication than other traditional screening procedures with a sensitivity rate of >99.9% for Down Syndrome, Edwards Syndrome and Patau Syndrome. NICC® significantly reduces the number of women undergoing unnecessary invasive diagnostic procedures. 

NICC® Screens for  
Down Syndrome (Trisomy 21)
Edwards Syndrome (Trisomy 18)
Patau Syndrome(Trisomy13)
Trisomy 9
Trisomy 16
Trisomy 22
Mircodeletion Syndromes:

DiGeorge Syndrome 2
Jacobsen Syndrome
Van der Woude Syndrome
Prader-Willi/Angelman Syndrome
Sex Chromosome Aneuploidies:
Turner Syndrome (XO)

Klinefelter Syndrome (XXY)
Triple-X Syndrome (XXX)
Jacob's Syndrome (XYY)
Male (XY)
Female (XX)

How does it work?

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.



  Frequently Asked Question (FAQ)


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