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XRCC2 Gene Fanconi Anemia XRCC2 Related Genetic Test

Original price was: $700.Current price is: $500.

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The XRCC2 Gene Fanconi Anemia NGS Genetic DNA Test is a comprehensive genetic analysis that detects mutations in the XRCC2 gene associated with Fanconi anemia, a rare inherited bone marrow failure syndrome. This advanced Next Generation Sequencing test provides precise identification of genetic variants that can lead to bone marrow failure, congenital abnormalities, and increased cancer risk. The test is crucial for individuals with family history of Fanconi anemia, unexplained bone marrow failure, or characteristic physical abnormalities. Results help guide medical management, inform treatment decisions, and provide valuable information for family planning. The test is available for $500 USD with a regular price of $700 USD, offering significant savings for comprehensive genetic insights.

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XRCC2 Gene Fanconi Anemia XRCC2 Related NGS Genetic DNA Test

Comprehensive Genetic Analysis for Fanconi Anemia Detection

The XRCC2 Gene Fanconi Anemia NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the XRCC2 gene, which plays a critical role in DNA repair mechanisms. Fanconi anemia is a rare inherited disorder characterized by bone marrow failure, congenital abnormalities, and increased susceptibility to cancers. This comprehensive genetic test utilizes Next Generation Sequencing technology to provide accurate and reliable results for individuals and families affected by or at risk for this condition.

What This Test Measures and Detects

This advanced genetic test specifically targets the XRCC2 gene, which encodes a protein essential for DNA repair through the Fanconi anemia pathway. The test identifies:

  • Pathogenic mutations in the XRCC2 gene
  • Single nucleotide variants and small insertions/deletions
  • Copy number variations affecting gene function
  • Inheritance patterns of Fanconi anemia
  • Genetic markers associated with disease severity and progression

Who Should Consider This Test

This genetic test is recommended for individuals presenting with:

  • Unexplained bone marrow failure or aplastic anemia
  • Family history of Fanconi anemia or related disorders
  • Characteristic physical abnormalities including short stature, skin pigmentation changes, or thumb abnormalities
  • Increased cancer risk at a young age, particularly leukemia or solid tumors
  • Developmental delays or congenital malformations
  • Planning for pregnancy with known family history of Fanconi anemia

Key Benefits of Genetic Testing

Undergoing the XRCC2 Gene Fanconi Anemia test provides numerous advantages:

  • Early Diagnosis: Enables prompt intervention and management strategies
  • Personalized Treatment: Guides appropriate medical care based on genetic findings
  • Family Planning: Provides crucial information for reproductive decisions
  • Cancer Risk Assessment: Identifies individuals requiring enhanced cancer surveillance
  • Comprehensive Care: Facilitates multidisciplinary approach involving hematologists, geneticists, and oncologists

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our expert genetic counselors and physicians:

  • Positive Result: Indicates the presence of a pathogenic mutation in the XRCC2 gene, confirming Fanconi anemia diagnosis
  • Negative Result: Suggests no detectable mutation in the XRCC2 gene, though other genetic causes may need consideration
  • Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further investigation
  • Carrier Status: Determines if an individual carries one copy of a mutated gene without showing symptoms

Test Details and Pricing

Test Component Details
Test Name XRCC2 Gene Fanconi Anemia XRCC2 Related NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next Generation Sequencing (NGS) Technology

Pre-Test Requirements

Before undergoing testing, we recommend:

  • Comprehensive clinical history documentation
  • Genetic counseling session to discuss implications and expectations
  • Development of a detailed family pedigree chart
  • Discussion of potential outcomes and their impact

Nationwide Accessibility

We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures accessible genetic testing services for patients throughout the country.

Take Control of Your Genetic Health

Don’t wait to get the answers you need about your genetic health. Early detection of Fanconi anemia through XRCC2 gene testing can significantly impact treatment outcomes and quality of life. Our team of genetic specialists is ready to guide you through the testing process and provide comprehensive support.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your XRCC2 Gene Fanconi Anemia NGS Genetic DNA Test. Take the first step toward understanding your genetic health and making informed medical decisions.