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
Accurate
99% accuracy for the detection of Down Syndrome, Edwards Syndrome and Patau Syndrome
Safe
NICC® is non-invasive, there is no risk of miscarriages
Protected
NICC® is covered by insurance and provides complimentary diagnostic test for high risk cases
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 | |
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Trisomies: Down Syndrome (Trisomy 21) Edwards Syndrome (Trisomy 18) Patau Syndrome(Trisomy13) Trisomy 9 Trisomy 16 Trisomy 22 |
Mircodeletion Syndromes: 1p36 2q33.1 16p12.2 Cri-du-chat DiGeorge Syndrome 2 Jacobsen Syndrome Van der Woude Syndrome Prader-Willi/Angelman Syndrome |
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Sex Chromosome Aneuploidies: Turner Syndrome (XO) Klinefelter Syndrome (XXY) Triple-X Syndrome (XXX) Jacob's Syndrome (XYY) |
Gender: Male (XY) Female (XX) |
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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.
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Frequently Asked Question (FAQ)  |
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