Non-Invasive Prenatal Test (NIPT)
- Non-Invasive Prenatal Screening
- Simple Maternal Blood Collection
- Advanced Genetic Screening
- Available From 10 Weeks
Results in: 8 Days
Sample: 10 mL Whole Blood in specialized Streck tube, Maternal blood only
What is Non-Invasive Prenatal Test (NIPT)?
NIPT (Non-Invasive Prenatal Testing) is a screening test performed during pregnancy to assess the risk of certain chromosomal abnormalities in the developing baby. It is done using a simple blood sample from the mother. The blood contains small fragments of DNA from the placenta, which are analysed to screen for selected chromosomal conditions.
Conditions Screened by NIPT
- Trisomy 21 (Down Syndrome)
- Trisomy 18 (Edwards Syndrome)
- Trisomy 13 (Patau Syndrome)
- Turner Syndrome (Monosomy X)
- Klinefelter Syndrome (XXY)
- Triple X Syndrome (XXX)
- XYY Syndrome
- Selected microdeletion syndromes (DiGeorge, 1p36, etc.)
Who May Consider Non-Invasive Prenatal Test (NIPT)
Women seeking early screening for common chromosomal conditions, regardless of age or risk factors.
Those with an increased age-related risk of chromosomal abnormalities.
Women with a previous pregnancy affected by chromosomal abnormalities
Women with a family history of chromosomal conditions
Women with abnormal first-trimester screening results
How Non-Invasive Prenatal Test (NIPT) Works
Trisomy 21 (Down Syndrome) Screening
Professional diagnostic services tailored to your specific clinical needs.
Trisomy 18 (Edwards Syndrome) Screening
Professional diagnostic services tailored to your specific clinical needs.
Trisomy 13 (Patau Syndrome) Screening
Professional diagnostic services tailored to your specific clinical needs.
Fetal Gender Determination (Optional)
Professional diagnostic services tailored to your specific clinical needs.
Our Simple 4 Step Process
Efficient • Reliable • Professional
Simple Collection
Blood collection from the mother as early as 10 weeks.
DNA Extraction
Extraction of cell-free fetal DNA from maternal blood.
Genomic Analysis
High-precision analysis using advanced molecular techniques.
Detailed Report
Screening results are reported with guidance for follow-up where needed.
Accuracy and Reliability
“NIPT is a highly accurate screening test for common chromosomal conditions. A high-risk result should be discussed with your healthcare provider and may require diagnostic confirmation.”
Choose Your Screening Panel
Select the right level of detailed screening
NIPT BASIC SCREEN
The Basic panel includes screening for the most common chromosomal conditions.
- Trisomy 21 (Down Syndrome)
- Trisomy 18 (Edwards Syndrome)
- Trisomy 13 (Patau Syndrome)
- Fetal Gender Determination
NIPT ADVANCED SCREEN
Expanded chromosomal analysis for comprehensive screening.
- Common Trisomies (21, 18, 13)
- Sex Chromosome Abnormalities (Turner, Klinefelter, XXX, XYY)
- Rare Autosomal Trisomies (9, 16, 22)
- Fetal Gender Determination
NIPT ADVANCED PLUS SCREEN WITH MICRODELETION
Our most detailed screening including microdeletion syndromes.
- Everything in Advanced Screen
- 22q11.2 Deletion Syndrome
- 1p36 Deletion Syndrome
- Angelman & Prader-Willi Syndrome
- Cri-du-chat Syndrome
- Optional Fetal Gender Determination
Frequently Asked Questions
Book Non-Invasive Prenatal Test (NIPT) Today
Contact our team to learn about this test and booking options.