Ensure the health of your baby with accurate and safe prenatal screening! At Forte Clinical Laboratory, we offer both NIPT Basic and Advanced panels at affordable prices with fast turnaround times (TAT).
- Safe & Non-Invasive: Just a simple blood test, with no risk to you or your baby.
- Accurate Results: Early detection of chromosomal abnormalities such as Down syndrome, Edwards syndrome, and Patau syndrome.
- Flexible Options: Choose from Basic or Advanced panels depending on your needs.
- Fast Turnaround Time: Get your results quickly without unnecessary delays.
- Affordable Pricing: High-quality testing at cost-effective rates.
💡 Why choose Forte?
With state-of-the-art technology, skilled professionals, and patient-focused service, Forte Clinical Laboratory is committed to reliable diagnostics for your peace of mind.
Book your NIPT test today and take the first step toward a healthy pregnancy!
Benefits of NIPT (Non-Invasive Prenatal Testing):
- Safe & Non-Invasive – Only requires a simple blood sample from the mother, with no risk to the baby.
- Early Detection – Can detect chromosomal abnormalities as early as 10 weeks of pregnancy.
- High Accuracy – Reliable screening for conditions such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13).
- Peace of Mind – Provides expectant parents with reassurance about their baby’s health.
- Quick Results – Fast turnaround time compared to traditional invasive tests.
- Minimal Stress – Non-invasive nature avoids the anxiety and risk associated with procedures like amniocentesis.
- Flexible Options – Available in Basic and Advanced panels to meet individual needs.
- Cost-Effective – Affordable pricing while maintaining high-quality, reliable testing.
NIPT Basic vs Advanced
| Feature | NIPT Basic | NIPT Advanced |
|---|---|---|
| Scope | Screens for common chromosomal abnormalities: Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), Patau syndrome (Trisomy 13) | Comprehensive screening for common and rare chromosomal abnormalities, including sex chromosome aneuploidies (X, Y abnormalities) and microdeletions |
| Target Audience | Standard-risk pregnancies or parents seeking basic screening | High-risk pregnancies, older maternal age, or those seeking a more detailed analysis |
| Detection Range | Limited to major trisomies | Expanded to include additional chromosomal abnormalities and microdeletions |
| Cost | More affordable | Higher cost due to extended analysis |
| Turnaround Time (TAT) | Fast | Slightly longer due to broader testing scope |
