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QF PCR Panel 13,18,21,XY Karyotyping

Original price was: $400.Current price is: $300.

-25%

The QF PCR Panel 13,18,21,XY Karyotyping is a sophisticated genetic diagnostic test that combines quantitative fluorescence polymerase chain reaction with traditional chromosome analysis. This comprehensive screening detects numerical abnormalities in chromosomes 13, 18, 21 and sex chromosomes (X and Y), providing crucial information about common chromosomal disorders. The test is particularly valuable for prenatal diagnosis, identifying conditions like Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13). Using advanced cell culture techniques and Sanger sequencing methodology, this dual-approach test offers both rapid preliminary results within 1-2 days and comprehensive analysis within 12-15 days. The test is available for $300 USD and requires samples including amniotic fluid, chorionic villi, or cord blood collected in specialized containers. This powerful genetic screening provides expectant parents and healthcare providers with essential information for informed decision-making about pregnancy management and future healthcare planning.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
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QF PCR Panel 13,18,21,XY Karyotyping: Comprehensive Chromosomal Analysis

Understanding Advanced Genetic Screening

The QF PCR Panel 13,18,21,XY Karyotyping represents a cutting-edge approach to chromosomal analysis that combines the speed of quantitative fluorescence polymerase chain reaction with the comprehensive nature of traditional karyotyping. This sophisticated diagnostic tool provides healthcare providers and patients with detailed insights into chromosomal health, particularly focusing on the most common chromosomal abnormalities that can impact development and health outcomes.

What This Test Measures and Detects

This comprehensive genetic screening specifically targets numerical abnormalities in four critical chromosomal regions:

  • Chromosome 13 Analysis: Detects trisomy 13 (Patau syndrome) associated with severe intellectual disability and physical abnormalities
  • Chromosome 18 Screening: Identifies trisomy 18 (Edwards syndrome) characterized by multiple congenital malformations
  • Chromosome 21 Evaluation: Screens for trisomy 21 (Down syndrome), the most common chromosomal disorder
  • Sex Chromosome Assessment: Analyzes X and Y chromosomes for numerical abnormalities including Turner syndrome, Klinefelter syndrome, and other sex chromosome variations

Who Should Consider This Genetic Screening

This advanced chromosomal analysis is particularly recommended for:

  • Pregnant Women with Abnormal Screening Results: Following abnormal first or second trimester screening tests
  • Advanced Maternal Age: Women aged 35 years or older at delivery
  • Family History Concerns: Individuals with family history of chromosomal disorders
  • Previous Affected Pregnancy: Couples with previous children or pregnancies with chromosomal abnormalities
  • Abnormal Ultrasound Findings: When ultrasound reveals structural abnormalities suggestive of chromosomal disorders
  • Recurrent Pregnancy Loss: Couples experiencing multiple miscarriages

Significant Benefits of Comprehensive Chromosomal Analysis

Choosing the QF PCR Panel 13,18,21,XY Karyotyping offers multiple advantages:

  • Dual-Method Reliability: Combines rapid QF-PCR results (1-2 days) with comprehensive karyotyping (12-15 days) for maximum accuracy
  • Early Detection Capability: Enables early identification of chromosomal abnormalities for timely medical interventions
  • Comprehensive Coverage: Screens for the most clinically significant chromosomal disorders in a single test
  • Informed Decision Making: Provides essential information for pregnancy management and family planning decisions
  • Reduced Anxiety: Offers clarity and reduces uncertainty about chromosomal health status

Understanding Your Test Results

Interpreting your chromosomal analysis results requires professional medical guidance:

  • Normal Results: Indicate typical chromosomal patterns with no detected abnormalities in the screened chromosomes
  • Abnormal Findings: May show additional copies of chromosomes (trisomy) or missing chromosomes (monosomy)
  • Mosaic Patterns: Some cells may show abnormalities while others appear normal, requiring specialized interpretation
  • Follow-up Recommendations: Abnormal results typically warrant genetic counseling and additional testing
  • Clinical Correlation: Results should always be interpreted in context with clinical findings and ultrasound results

Test Pricing Information

Test Description Price (USD)
QF PCR Panel 13,18,21,XY Karyotyping – Discount Price $300
QF PCR Panel 13,18,21,XY Karyotyping – Regular Price $400

Nationwide Accessibility

We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, 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 genetic testing services nationwide.

Take the Next Step in Genetic Health

Don’t leave your genetic health questions unanswered. Our team of genetic specialists and certified laboratory professionals are ready to provide you with the comprehensive chromosomal analysis you need for informed healthcare decisions. Schedule your QF PCR Panel 13,18,21,XY Karyotyping today and gain the clarity that advanced genetic testing can provide.

Call or WhatsApp us now at +1(267) 388-9828 to book your appointment or discuss your testing needs with our genetic counseling team.

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