QF PCR Panel 13,18,21,XY – Comprehensive Prenatal Genetic Testing
Understanding the QF PCR Panel 13,18,21,XY Test
The QF PCR Panel 13,18,21,XY represents a cutting-edge advancement in prenatal genetic diagnostics, offering rapid and accurate detection of the most common chromosomal abnormalities affecting fetal development. This sophisticated molecular test utilizes Quantitative Fluorescent Polymerase Chain Reaction (QF-PCR) technology to analyze chromosomes 13, 18, 21, and the sex chromosomes, providing crucial information that helps guide pregnancy management decisions.
What Does the Test Measure and Detect?
This comprehensive panel specifically targets and identifies:
- Trisomy 21 (Down Syndrome): Extra copy of chromosome 21
- Trisomy 18 (Edwards Syndrome): Extra copy of chromosome 18
- Trisomy 13 (Patau Syndrome): Extra copy of chromosome 13
- Sex Chromosome Abnormalities: Including Turner syndrome, Klinefelter syndrome, and other X/Y chromosome variations
- Chromosomal Aneuploidies: Abnormal number of chromosomes in developing fetus
Who Should Consider This Test?
The QF PCR Panel 13,18,21,XY is recommended for:
- Pregnant women with abnormal ultrasound findings
- Expectant mothers with positive first-trimester screening results
- Women with advanced maternal age (35 years or older)
- Couples with family history of chromosomal disorders
- Previous pregnancy with chromosomal abnormalities
- Cases where rapid results are clinically necessary
Clinical Indications and Symptoms
Healthcare providers typically recommend this test when:
- Ultrasound reveals structural abnormalities
- Nuchal translucency measurements are increased
- There are concerns about fetal growth and development
- Multiple marker screening indicates elevated risk
- Family planning requires comprehensive genetic information
Benefits of QF PCR Panel Testing
Choosing the QF PCR Panel 13,18,21,XY offers numerous advantages:
- Rapid Results: Receive comprehensive genetic information within 1-2 days
- High Accuracy: Advanced Sanger Sequencing technology ensures reliable results
- Comprehensive Screening: Covers the most clinically significant chromosomal abnormalities
- Early Intervention: Enables timely medical decisions and appropriate care planning
- Peace of Mind: Provides clarity and reduces uncertainty during pregnancy
- Cost-Effective: Affordable testing with significant clinical value
Test Methodology and Technology
Our QF PCR Panel utilizes state-of-the-art Sanger Sequencing methodology, which represents the gold standard in genetic analysis. This technique provides:
- Precise detection of chromosomal copy number variations
- High sensitivity and specificity for targeted chromosomes
- Reliable results even with limited sample material
- Comprehensive quality control measures
- Expert interpretation by certified genetic specialists
Understanding Your Test Results
Your QF PCR Panel results will be carefully interpreted by our team of genetic specialists:
Normal Results
A normal result indicates that no abnormalities were detected in chromosomes 13, 18, 21, or the sex chromosomes. This significantly reduces the likelihood of the targeted chromosomal conditions, though it doesn’t eliminate all possible genetic concerns.
Abnormal Results
If abnormalities are detected, our genetic counselors will provide:
- Detailed explanation of the specific findings
- Clinical implications and potential outcomes
- Guidance on next steps and additional testing options
- Referrals to appropriate specialists if needed
- Emotional support and counseling resources
Follow-up and Genetic Counseling
All abnormal results include complimentary genetic counseling sessions to help you understand the findings and make informed decisions about your pregnancy management.
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $150 |
| Regular Price | $200 |
| Turnaround Time | 1-2 Days |
| Sample Type | Amniotic Fluid / Chorionic Villi / Cord Blood |
Sample Collection and Requirements
The test requires specific sample types collected by qualified healthcare professionals:
- Amniotic Fluid: Collected via amniocentesis procedure
- Chorionic Villi: Obtained through chorionic villus sampling (CVS)
- Cord Blood: Collected during specific prenatal procedures
Nationwide Testing Availability
We proudly offer the QF PCR Panel 13,18,21,XY testing services across the United States, with convenient locations in all major cities including:
- New York City, NY
- Los Angeles, CA
- Chicago, IL
- Houston, TX
- Phoenix, AZ
- Philadelphia, PA
- San Antonio, TX
- San Diego, CA
- Dallas, TX
- San Jose, CA
Prescription Requirements
Please note that the QF PCR Panel 13,18,21,XY requires a doctor’s prescription. Prescription requirements do not apply for surgery and pregnancy cases or individuals planning to travel abroad.
Book Your Test Today
Take the first step toward comprehensive prenatal genetic screening. Our experienced team is ready to assist you with scheduling, sample collection coordination, and answering any questions you may have about the QF PCR Panel 13,18,21,XY.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or learn more about this essential prenatal genetic test.
Our genetic specialists are available to discuss your testing needs, explain the procedure in detail, and help you understand how this advanced screening can provide valuable insights into your pregnancy health.
