The Ultimate NICC Test (NIPT) is our most comprehensive non-invasive prenatal test (NIPT), designed for expectant parents who want the highest level of genetic screening available during pregnancy.
Using a simple maternal blood sample, this advanced NIPT analyses fetal cell-free DNA (cfDNA) and can be performed from 10 weeks of pregnancy onwards, with no risk to the baby.
Screens for common chromosomal trisomies, including:
• Trisomy 21 (Down Syndrome)
• Trisomy 18 (Edwards Syndrome)
• Trisomy 13 (Patau Syndrome)
(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
(Microdeletion Analysis)
Screens for selected clinically significant microdeletion syndromes, including:
• DiGeorge Syndrome (22q11.2 Deletion)
• Angelman Syndrome
• Prader–Willi Syndrome
• Cri-du-Chat Syndrome
• 1p36 Deletion Syndrome
The Ultimate NICC NIPT includes expanded screening for 25 single-gene disorders in the baby, covering conditions such as:
• Skeletal disorders
• Noonan spectrum disorders
• Craniosynostosis syndromes
• Syndromic genetic disorders
These conditions may not always be detected through early ultrasound alone.
(Maternal Carrier Screening)
Includes screening for 18 single-gene recessive disorders in the mother, such as:
Alpha Thalassemia, Beta Thalassemia, G6PD Deficiency, Galactosemia, Phenylketonuria, Citrin Deficiency, Pompe Disease, Wilson Disease, 5 Alpha-reductase Deficiency, Pendred Syndrome, Primary Carnitine Deficiency, Niemann-Pick Disease, Cystic Fibrosis, Charcot–Marie–Tooth Disease, Polycystic Kidney Disease, Hemophilia A, Adrenoleukodystrophy, and Ornithine Transcarbamylase Deficiency.
Fetal gender can be identified from 10 weeks onwards,
A detailed consultation with our Klinik Caring doctors to:
• Explain your NIPT results clearly
• Discuss clinical significance and implications
• Advise on further testing or specialist referral if needed
The Ultimate NICC Test (NIPT) in Johor Bahru is ideal for parents who want maximum reassurance and the most detailed prenatal genetic screening available.
It is commonly chosen by parents who:
• Want the most comprehensive NIPT option
• Have a family history of genetic conditions
• Have previous pregnancy concerns
• Prefer early, in-depth genetic insight
• Want both fetal and maternal genetic screening
This non-invasive NIPT blood test is safe, accurate, and poses no miscarriage risk, while fitting seamlessly into routine antenatal care.
At Klinik Caring, we focus on clear explanations, thoughtful counselling, and supporting parents through informed decision-making.
The Ultimate NICC Test is a comprehensive non-invasive prenatal test (NIPT) that combines fetal chromosomal screening, microdeletion analysis, expanded single-gene disorder screening, and maternal genetic carrier screening.
The test can be done from 10 weeks of pregnancy onwards.
Yes. It is performed using a maternal blood sample only and does not increase miscarriage risk.
Ultimate NICC includes everything in Advanced and Advanced Plus, and additionally screens for expanded single-gene disorders in the baby, making it the most comprehensive option.
No. NIPT is a screening test and does not replace routine ultrasound scans or standard antenatal check-ups.
Our doctors will discuss the findings carefully and guide you on appropriate next steps, which may include further testing or specialist referral.
The Ultimate NICC Test (NIPT) is available at Klinik Caring, serving patients from Skudai, Impian Emas, and across Johor Bahru.
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