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FANCB Gene Fanconi Anemia Type B Genetic Test

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

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The FANCB Gene Fanconi Anemia Type B NGS Genetic DNA Test is a comprehensive diagnostic tool that identifies mutations in the FANCB gene responsible for Fanconi anemia type B. This next-generation sequencing test provides detailed analysis of genetic variations that can lead to bone marrow failure, congenital abnormalities, and increased cancer susceptibility. The test is particularly valuable for individuals with family history of Fanconi anemia, unexplained bone marrow failure, or characteristic physical features associated with the condition. Results help guide medical management, inform family planning decisions, and enable early intervention strategies. The test is priced at $500 USD and provides crucial genetic information for patients and healthcare providers managing this rare inherited disorder.

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FANCB Gene Fanconi Anemia Type B NGS Genetic DNA Test

Comprehensive Genetic Analysis for Fanconi Anemia Detection

The FANCB Gene Fanconi Anemia Type B NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the FANCB gene, which is responsible for Fanconi anemia type B. This rare inherited disorder affects the body’s ability to repair DNA damage and can lead to serious health complications including bone marrow failure, congenital abnormalities, and increased cancer risk. Our advanced next-generation sequencing technology provides comprehensive analysis of the entire FANCB gene, ensuring accurate detection of even the most subtle genetic variations.

What Does the FANCB Gene Test Measure?

This specialized genetic test specifically targets and analyzes the FANCB gene located on the X chromosome. The test detects:

  • Point mutations, deletions, and insertions in the FANCB gene
  • Genetic variations that disrupt the Fanconi anemia DNA repair pathway
  • Inherited mutations that can cause bone marrow failure syndrome
  • Genetic markers associated with increased cancer susceptibility
  • Variants that may impact treatment response and medical management

Who Should Consider This Genetic Test?

This test is particularly recommended for individuals exhibiting:

  • Unexplained bone marrow failure or aplastic anemia
  • Family history of Fanconi anemia or related genetic disorders
  • Characteristic physical features including short stature, skin pigmentation abnormalities, or thumb and arm anomalies
  • Developmental delays or congenital malformations
  • Increased chromosomal breakage in laboratory testing
  • Planning for family and reproductive decisions with known family history

Significant Benefits of FANCB Genetic Testing

Undergoing FANCB gene testing provides numerous advantages for patients and families:

  • Early Diagnosis: Enables prompt intervention and management strategies
  • Family Planning: Provides crucial information for reproductive decision-making
  • Personalized Care: Guides targeted monitoring for cancer and bone marrow complications
  • Treatment Guidance: Informs appropriate therapeutic approaches and avoids harmful treatments
  • Genetic Counseling: Supports comprehensive family risk assessment and management

Understanding Your Test Results

Our comprehensive genetic report provides clear interpretation of your FANCB gene analysis:

  • Positive Result: Indicates the presence of a pathogenic mutation in the FANCB gene, confirming Fanconi anemia type B diagnosis
  • Negative Result: Suggests no detectable FANCB gene mutations, though does not completely rule out other genetic causes
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
  • Carrier Status: Determines if individuals carry one copy of a mutated gene without showing symptoms

All results are accompanied by detailed explanations and recommendations for follow-up care with genetic specialists.

Test Pricing and Details

Test Feature Details
Test Name FANCB Gene Fanconi Anemia Type B 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

Nationwide Testing Availability

GGC DNA maintains comprehensive testing facilities across the United States, with convenient locations in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic counselors and medical professionals ensures accessible, high-quality genetic testing services nationwide.

Take Control of Your Genetic Health Today

Don’t wait to get the answers you need about Fanconi anemia risk and genetic health. Our FANCB Gene Fanconi Anemia Type B NGS Genetic DNA Test provides the comprehensive genetic information necessary for informed medical decisions and proactive health management. Schedule your test today and take the first step toward understanding your genetic profile.

Call or WhatsApp us now at +1(267) 388-9828 to book your FANCB genetic test or to speak with our genetic counseling team. Early detection through genetic testing can make a significant difference in managing Fanconi anemia and related health risks.