Description
Pregnancy NIPT Test and Cost for Common Trisomies and : Down Syndrome, Edwards Syndrome & Patau Syndrome Screening
Comprehensive Prenatal Screening for Chromosomal Abnormalities
The Standard Non-Invasive Prenatal Test (NIPT) is a cutting-edge blood-based screening method designed to detect chromosomal abnormalities in developing fetuses with exceptional accuracy. Priced at ₹10,000 in India, this test analyzes cell-free fetal DNA circulating in the mother’s bloodstream to assess risks for Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), and Trisomy 13 (Patau syndrome). Unlike invasive procedures like amniocentesis, NIPT poses zero risk of miscarriage and delivers results with over 99% sensitivity for these conditions.
Conditions Screened by NIPT Test
Trisomy 21 (Down Syndrome)
Down syndrome, caused by an extra copy of chromosome 21, is the most common chromosomal disorder, affecting approximately 1 in 800 live births. It is associated with intellectual disabilities, distinct facial features, and increased risk of congenital heart defects. The Standard NIPT identifies Trisomy 21 with over 99% detection rates, significantly outperforming traditional first-trimester combined screening methods.
Trisomy 18 (Edwards Syndrome)
Edwards syndrome involves an extra chromosome 18 and occurs in 1 in 5,000 live births. Affected infants often have severe developmental delays, heart defects, and a life expectancy rarely exceeding one year. NIPT detects Trisomy 18 with 98–99% accuracy, enabling early counseling for families.
Trisomy 13 (Patau Syndrome)
Patau syndrome, caused by an extra chromosome 13, affects 1 in 16,000 newborns and leads to life-threatening organ malformations. The Standard NIPT screens for this condition with 95–99% sensitivity, providing critical insights for prenatal care planning.
Why Choose Standard NIPT Test?
Key Benefits for Indian Patients
- Safety: No risk of miscarriage compared to invasive tests like amniocentesis.
- Early Detection: Conducted from 9–10 weeks of gestation, far earlier than anatomy scans.
- Accuracy: Reduces false positives by 90% compared to traditional serum screenings.
- Affordability: Priced at ₹10,000, it is India’s most cost-effective advanced prenatal screen.
Who Should Consider This Test?
The Standard NIPT is recommended for:
- Women aged 35+ (advanced maternal age increases trisomy risks).
- Pregnancies with abnormal ultrasound findings or serum screening results.
- Families with a history of chromosomal disorders.
- Any expecting parent seeking peace of mind through early, reliable screening.
Test Process & Reporting
Simple 3-Step Procedure
- Consultation: A healthcare provider reviews medical history and gestational age.
- Blood Draw: A single blood sample is collected from the mother’s arm (no fasting required).
- Analysis: Advanced sequencing detects fetal DNA fragments and evaluates chromosomal ratios.
Results are typically available within 7–10 days, reported as “Low Probability” or “High Probability” for each condition. For high-probability results, diagnostic confirmation via amniocentesis is advised.
NIPT Test Cost & Accessibility in India
Priced at ₹10,000, the Standard NIPT is widely accessible across major cities like Mumbai, Delhi, Bangalore, and Hyderabad. NIPT Test lab offer free home sample collection, making it convenient for rural and urban patients alike.
Comparing NIPT to Traditional Methods
| Feature | Standard NIPT | First-Trimester Screening |
|---|---|---|
| Detection Rate (T21) | Over 99% | 85–90% |
| False Positive Rate | Less than 1% | 2–7% |
| Procedure Risk | None | None |
| Gestational Age | 9+ weeks | 11–13 weeks |
Frequently Asked Questions
Is NIPT Test Reliable for Low-Risk Pregnancies?
Yes. Studies confirm over 99% sensitivity for Trisomy 21 across all risk groups, making it suitable for low-risk pregnancies.
When Should I Schedule the Test?
Optimal testing occurs between 9–12 weeks to allow time for confirmatory diagnostics if needed.
What If Results Are Positive?
A “High Probability” result requires confirmation via amniocentesis or CVS. Genetic counselors help interpret results and guide next steps.
Conclusion
The Pregnancy NIPT at ₹10,000 is India’s gold standard for early, safe, and accurate prenatal screening. By focusing on Trisomy 21, 18, and 13, it empowers expecting parents with actionable insights while avoiding the risks of invasive procedures. With same-day sample collection and rapid turnaround, this test redefines prenatal care accessibility nationwide.
Leave feedback about this