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IRF8 Gene Immunodeficiency Type 32B Monocyte and Dendritic Cell Deficiency Autosomal Recessive NGS Genetic DNA Test

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

-29%

The IRF8 Gene Immunodeficiency Type 32B NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the IRF8 gene responsible for rare autosomal recessive immune disorders. This comprehensive test specifically detects deficiencies in monocyte and dendritic cell development, which are crucial components of the immune system. Using next-generation sequencing technology, our test provides precise genetic analysis for patients experiencing recurrent infections, immune system abnormalities, and related symptoms. The test costs $500 USD and offers valuable insights for proper diagnosis, treatment planning, and genetic counseling. Early detection through this test can significantly improve patient outcomes and guide appropriate medical interventions for affected individuals and families.

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IRF8 Gene Immunodeficiency Type 32B Monocyte and Dendritic Cell Deficiency Autosomal Recessive NGS Genetic DNA Test

Understanding IRF8 Gene Immunodeficiency Type 32B

The IRF8 Gene Immunodeficiency Type 32B test represents a breakthrough in genetic diagnostics for rare immune disorders. This specialized Next-Generation Sequencing (NGS) test specifically targets mutations in the IRF8 (Interferon Regulatory Factor 8) gene, which plays a critical role in the development and function of monocytes and dendritic cells – essential components of your body’s immune defense system.

What Does This Test Measure?

Our advanced NGS genetic DNA test precisely identifies:

  • Pathogenic variants in the IRF8 gene responsible for autosomal recessive inheritance
  • Specific mutations affecting monocyte and dendritic cell development
  • Genetic markers associated with immunodeficiency type 32B
  • Inheritance patterns to determine carrier status and recurrence risks

Who Should Consider This Test?

This genetic test is particularly recommended for individuals experiencing:

  • Recurrent and severe bacterial, viral, or fungal infections
  • Unexplained immune system deficiencies
  • Family history of IRF8-related disorders
  • Abnormal blood cell counts affecting monocytes
  • Diagnostic challenges in immune system evaluation
  • Children with developmental immune abnormalities

Clinical Symptoms and Indications

Patients with IRF8 Gene Immunodeficiency Type 32B often present with:

  • Chronic respiratory infections and pneumonia
  • Skin manifestations and dermatological conditions
  • Increased susceptibility to opportunistic infections
  • Delayed wound healing and tissue repair issues
  • Autoimmune-like symptoms despite immunodeficiency
  • Growth and developmental concerns in pediatric cases

Benefits of IRF8 Genetic Testing

Choosing our comprehensive genetic analysis provides numerous advantages:

  • Accurate Diagnosis: Precise identification of IRF8 gene mutations eliminates diagnostic uncertainty
  • Personalized Treatment: Results guide targeted therapeutic approaches and management strategies
  • Family Planning: Enables informed reproductive decisions and genetic counseling
  • Early Intervention: Facilitates proactive medical care before severe complications develop
  • Comprehensive Analysis: NGS technology ensures thorough examination of the entire IRF8 gene

Understanding Your Test Results

Our genetic specialists provide detailed interpretation of your results:

  • Positive Result: Indicates presence of IRF8 gene mutations; our genetic counselors will explain implications and next steps
  • Negative Result: Suggests absence of tested mutations; however, clinical correlation remains essential
  • Variant of Uncertain Significance: Requires additional family studies and clinical evaluation
  • Carrier Status: Identifies individuals who may pass the condition to offspring

Test Details and Pricing

Test Component Details
Test Name IRF8 Gene Immunodeficiency Type 32B Monocyte and Dendritic Cell Deficiency Autosomal Recessive 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 scheduling your test, please ensure:

  • Complete clinical history documentation
  • Genetic counseling session to create family pedigree chart
  • Discussion of testing implications with healthcare provider
  • Understanding of potential outcomes and their significance

Nationwide Testing Availability

We proudly serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our state-of-the-art laboratories ensure consistent, reliable results regardless of your location.

Take Action Today

Don’t let uncertainty about your immune health continue. Our specialized genetic testing provides the clarity needed for proper diagnosis and treatment planning. Contact our genetic specialists today to schedule your IRF8 Gene Immunodeficiency Type 32B test and take the first step toward understanding your genetic health.

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