NIPT Advanced for 23 Chromosomes: Comprehensive Prenatal Screening
Understanding Advanced Non-Invasive Prenatal Testing
NIPT Advanced for 23 Chromosomes represents the cutting edge of prenatal screening technology, offering expectant parents unprecedented insight into their baby’s chromosomal health. This revolutionary test utilizes advanced DNA sequencing to analyze cell-free fetal DNA circulating in the mother’s bloodstream, providing comprehensive screening across all 23 chromosome pairs without any risk to the pregnancy.
What Does This Test Measure and Detect?
The NIPT Advanced for 23 Chromosomes test provides comprehensive screening for:
- Common Trisomies: Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13)
- Sex Chromosome Abnormalities: Turner syndrome, Klinefelter syndrome, Triple X syndrome, and XYY syndrome
- Microdeletion Syndromes: Detection of smaller chromosomal deletions that can cause significant health conditions
- All 23 Chromosome Pairs: Comprehensive screening across the entire chromosomal spectrum
- Fetal Fraction Analysis: Measurement of the amount of fetal DNA in maternal blood to ensure test accuracy
Who Should Consider NIPT Advanced Testing?
This advanced prenatal screening is recommended for:
- Women aged 35 years or older at delivery
- Patients with abnormal first-trimester screening results
- Those with ultrasound findings suggesting increased risk
- Couples with a family history of chromosomal abnormalities
- Previous pregnancy affected by chromosomal conditions
- Any expectant parent seeking comprehensive chromosomal screening
- Patients with elevated risk based on maternal serum screening
Key Benefits of NIPT Advanced for 23 Chromosomes
- Exceptional Accuracy: Over 99% detection rate for common trisomies with very low false-positive rates
- Early Detection: Available as early as 10 weeks of pregnancy
- Non-Invasive Procedure: Simple blood draw with no risk to mother or baby
- Comprehensive Screening: Covers all 23 chromosome pairs for complete assessment
- Rapid Results: Quick turnaround time for timely decision-making
- Peace of Mind: Provides valuable information to guide pregnancy management
Understanding Your Test Results
Your NIPT Advanced results will fall into one of several categories:
- Low Risk: Indicates a very low probability of the screened chromosomal conditions
- High Risk: Suggests increased likelihood of specific chromosomal abnormalities
- No Result: May occur due to low fetal fraction or technical factors, requiring repeat testing
- Atypical Finding: May indicate findings that require further evaluation
It’s important to understand that NIPT is a screening test, not a diagnostic test. High-risk results should be confirmed through diagnostic testing such as amniocentesis or chorionic villus sampling. Our genetic counselors are available to help you understand your results and discuss next steps.
Test Pricing Information
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $326 |
| Regular Price | $500 |
Nationwide Availability Across the United States
We have convenient testing locations throughout the United States, including major metropolitan areas such as New York City, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network of certified collection centers ensures accessible testing no matter where you’re located.
Take the Next Step Toward Peace of Mind
Don’t leave your baby’s chromosomal health to chance. The NIPT Advanced for 23 Chromosomes test provides the comprehensive screening you need for informed pregnancy decisions. Our experienced healthcare team is ready to guide you through the testing process and help you understand your results.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your NIPT Advanced test and take advantage of our special discounted pricing of only $326 USD. Our friendly staff will help you find the most convenient testing location and answer any questions you may have about this important prenatal screening.
