NICC Test

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NICC Test (Non-Invasive Chromosomal Check)

The NICC Test, or Non-Invasive Chromosomal Check, is a simple blood test that screens for certain genetic and chromosomal conditions in your baby. It is completely safe for both mother and baby because it does not involve any needle or instrument entering the womb.
At Klinik Caring, Impian Emas, we offer the NICC test to help expecting parents gain peace of mind through early and accurate screening. This test can be done as early as 10 weeks of pregnancy.

Why the NICC Test Is Important

Every baby has chromosomes that carry genetic information. Sometimes, extra or missing chromosomes can cause certain conditions. The NICC test helps to detect these risks early, without any harm to you or your baby.

The NICC Test Screens For:

Down Syndrome (Trisomy 21) – may cause learning difficulties and slower development
Edwards Syndrome (Trisomy 18) – may affect growth and organ function
Patau Syndrome (Trisomy 13) – may cause severe developmental issues
Sex Chromosome Conditions such as Turner or Klinefelter Syndrome
Microdeletions or rare chromosomal abnormalities (depending on the panel chosen)

While this is not a diagnostic test, it provides a highly accurate early screening so that further evaluation can be arranged if needed.

Find Out Our NICC Packages

At Klinik Caring, we offer three tiers of NICC packages to suit your needs:

Basic Package – screens for the most common trisomy conditions
Standard Package – includes additional sex chromosome analysis
Advanced Package – offers extended screening for microdeletions and rare chromosomal abnormalities

👉 Click here to learn more about our NICC packages

When the NICC Test Is Done

The NICC test can be performed from 10 weeks of pregnancy onward. It is usually recommended for:

Mothers aged 35 years and above
Pregnancies with abnormal ultrasound findings
Family history of genetic conditions
Parents who wish for early reassurance

How the Test Is Done

A small blood sample is taken from the mother’s arm.
The sample is sent to a specialised laboratory for analysis.
The laboratory examines the baby’s DNA fragments that circulate naturally in the mother’s blood.
The results are usually available within one to two weeks.

No fasting or special preparation is required.

What to Expect

The procedure feels like an ordinary blood test.
There is no risk to the baby.
Results are explained clearly by our doctor, including what they mean and whether any further testing is necessary.
The test can also determine your baby’s gender if you wish to know.

Frequently Asked Questions (FAQ) – NICC Test

1. Is the NICC test safe for me and my baby?
Yes. The NICC test is completely safe and non-invasive. It only requires a blood sample from the mother.

2. What is the difference between the NICC test and an amniocentesis?
The NICC test is a screening test that carries no risk to the baby, while amniocentesis is a diagnostic test that involves a small needle entering the womb and carries a very small risk of miscarriage.

3. When should I consider taking this test?
It can be taken as early as 10 weeks of pregnancy. It is suitable for all mothers who want early reassurance, especially those with higher risk factors.

4. Can the NICC test confirm that my baby is completely healthy?
No. The NICC test screens for the most common chromosomal conditions. It cannot detect all genetic or physical problems, but it is one of the most accurate early screening tools available.

5. Can the NICC test reveal my baby’s gender?
Yes. If requested, the test can also determine your baby’s gender accurately.