The Standard NICC Test (NIPT) is a non-invasive prenatal test (NIPT) that screens for common chromosomal abnormalities in the baby using a simple maternal blood sample. It analyses fetal cell-free DNA (cfDNA) and can be performed from 10 weeks of pregnancy onwards.
This test is a popular first-line NIPT screening option for expectant parents who want reliable, early reassurance.
Screens for common chromosomal trisomies, including:
• Trisomy 21 (Down Syndrome)
• Trisomy 18 (Edwards Syndrome)
• Trisomy 13 (Patau Syndrome)
• Trisomy 9, 16, and 22
(Sex Chromosome Abnormalities)
Screens for abnormalities involving sex chromosomes, including:
• Turner Syndrome (XO)
• Triple X Syndrome (XXX)
• Klinefelter Syndrome (XXY)
• Jacob’s Syndrome (XYY)
• Plus 22 other chromosomal aneuploidies
Fetal gender can be identified from 10 weeks onwards,
A consultation with our Klinik Caring doctors to:
• Explain your NIPT results clearly
• Discuss what the findings mean
• Advise on follow-up if required
The Standard NICC Test (NIPT) is ideal for parents who want a safe, accurate, and non-invasive prenatal screening without extended genetic testing.
It is commonly chosen by parents who:
• Want early screening for common chromosomal conditions
• Prefer a straightforward and reliable NIPT option
• Have no known genetic risk factors
• Want peace of mind from 10 weeks onwards
This non-invasive NIPT blood test poses no risk to the baby and fits well into routine antenatal care.
At Klinik Caring, we ensure every patient understands their results clearly and feels supported throughout their pregnancy journey.
Standard NICC is a non-invasive prenatal test (NIPT) that screens for common chromosomal abnormalities, including Down syndrome, Edwards syndrome, and Patau syndrome.
The Standard NICC Test can be done from 10 weeks of pregnancy onwards.
Yes. It is a simple blood test taken from the mother and carries no miscarriage risk.
The key difference is maternal genetic screening.
• Standard NICC (NIPT)
Screens the baby for common chromosomal abnormalities and sex chromosome conditions only.
• Standard Plus NICC (NIPT)
Includes almost everything in Standard NICC plus maternal screening for 18 single-gene recessive disorders, such as thalassemia and G6PD deficiency.
If you mainly want basic fetal chromosomal screening, Standard NICC is usually sufficient.
If you would also like to assess genetic carrier risks in the mother, Standard Plus NICC offers added reassurance.
No. NIPT is a screening test and does not replace routine ultrasound scans or standard antenatal check-ups.
The Standard NICC Test (NIPT) is available at Klinik Caring, serving patients from Skudai, Impian Emas, and the wider Johor Bahru area.
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