“Safe for Baby, Peace of Mind for Mommy”
Hello, A safer test for your baby! No more needles on mommy’s tummy…
Non-Invasive ChromosomesCheck (NICC) New and simple blood test for common chromosomal abnormalities detection
The risk of having a child with chromosomal abnormalities, such as Down syndrome (Trisomy 2 I ), Edward syndrome (Trisomy 18) and Patau syndrome (Trisomy 13) increases with age. Diagnostic tests for trisomies detection such as amniocentesis and chorionic villus sampling (CVS) are invasive and impose a risk of miscarriage to the pregnancy.
You can now avoid this risk with NICC test that can be done any time after 12 weeks of pregnancy. NICC is a simple, safe and accurate test for common chromosomal abnormalities detection.
Advantages of NICC
Simple – Requires only mother’s blood sample.
Safe – Non-invasive, and therefore no risk to the baby.
Accurate – It detects more than 99% of Down syndrome, Edward syndrome and Patau syndrome.
Who should consider NICC?
- Women with advanced maternal age (35 years old and above)
- Personal or family history of birth defects
- Previous birth of a child with a birth defect
- Positive serum screening test Abnormal ultrasound scan findings
Adapted from Non-invasive chromosomes check (NICC) Copyright 2013 DNA Laboratories Sdn. Bhd. All Rights Reserved. SP-BR.) 9 REV 01
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