Reliable Choice:
MomGuard NIPT
From the 9-10th week of pregnancy, detect genetic anomalies with 99.8% accuracy without leaving your home.
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Audio summary about the MomGuard test
This podcast episode was prepared with AI assistance. The expressions in the content may occasionally have shortcomings or linguistic errors. The information here is for general informational purposes only; it does not constitute a diagnosis or treatment recommendation. For any evaluation and decision regarding your health condition, please consult your physician or Omega Genetik Diagnostic Evaluation Center.
What is MomGuard NIPT?
The MomGuard test is a modern prenatal screening test developed by LabGenomics. It provides a definitive answer about your baby's genetic health early in pregnancy (from the 10th week).
It is a safe option for advanced maternal age pregnancies, those with risky screening test results, or all expectant mothers who just want peace of mind. Unlike invasive procedures like amniocentesis, it causes no harm to the baby.
How Does It Work?
During pregnancy, the baby's DNA fragments mix into the mother's blood (cffDNA). MomGuard analyzes this DNA from a simple blood sample from the mother to examine chromosome counts.
NGS Technology & Illumina
Next-Generation Sequencing
DNA isolated from the blood sample is read millions of times and analyzed using the Next Generation Sequencing (NGS) method with Illumina devices.
Bioinformatic Analysis
The obtained sequencing data is scanned with LabGenomics' advanced algorithms. Numerical chromosome anomalies are detected with AI support.
High Accuracy
Clinical validation studies have proven that MomGuard has a sensitivity above 99.8% in detecting Trisomy 21 (Down Syndrome).
What Does MomGuard Detect?
Trisomy 21
Known as Down Syndrome. The most common chromosome anomaly.
Trisomy 18
Edwards Syndrome. Causes serious developmental problems.
Trisomy 13
Patau Syndrome. A rare but serious anomaly.
Sex Chromosome Anomalies
Sex chromosome disorders such as Turner, Klinefelter.
Deletion/Microdeletion
Optional: DiGeorge, Angelman, Prader-Willi, Jacobsen, Cri-du-chat and 105+ other syndromes.
Documents and Sample Reports
You can download our brochure and sample reports for detailed information.
Easy Process in 4 Steps
Reliable results without fatigue or stress.
1. Book an Appointment
Choose a suitable time on nipt.tr.
2. At-Home Sample
Omega Care nurse comes to your address.
3. Analysis
Your sample is examined in our laboratory (10-14 days).
4. Result
Your report is delivered with expert explanation.
Why MomGuard?
| Feature | Double/Triple Screening | MomGuard NIPT | Amniocentesis |
|---|---|---|---|
| Accuracy Rate | %70 - %85 | %99.8 | %99,9 |
| Miscarriage Risk | None | None (Safe) | Yes (1/200) |
| Method | Blood + Ultrasound | Mother's Blood Only | Abdominal Needle |
| Timing | Weeks 11-14 | From Week 10 | 16+ Weeks |
Who Is It Suitable For?
Frequently Asked Questions
Meet MomGuard
Book your appointment now for a reliable, fast, and risk-free NIPT experience.
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