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RAC2 Gene Neutrophil Immunodeficiency Syndrome NGS Genetic DNA Test

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

-29%

The RAC2 Gene Neutrophil Immunodeficiency Syndrome NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the RAC2 gene responsible for severe neutrophil dysfunction and immunodeficiency disorders. This comprehensive test utilizes next-generation sequencing technology to provide accurate detection of pathogenic variants that disrupt normal immune cell function. Patients experiencing recurrent infections, poor wound healing, or autoimmune manifestations benefit from this precise diagnostic tool. The test costs $500 USD and delivers results within 3-4 weeks, enabling healthcare providers to develop targeted treatment strategies and improve patient outcomes through personalized medical interventions based on genetic findings.

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RAC2 Gene Neutrophil Immunodeficiency Syndrome NGS Genetic DNA Test

Comprehensive Genetic Analysis for Immune System Disorders

The RAC2 Gene Neutrophil Immunodeficiency Syndrome NGS Genetic DNA Test represents a breakthrough in diagnostic precision for individuals suffering from complex immune system disorders. This advanced genetic screening utilizes next-generation sequencing technology to identify mutations in the RAC2 gene, which plays a critical role in neutrophil function and overall immune response coordination. Neutrophils serve as the body’s first line of defense against infections, and disruptions in their activity can lead to severe immunodeficiency conditions requiring specialized medical intervention.

What This Revolutionary Test Detects

Our comprehensive NGS-based analysis specifically targets the RAC2 gene, examining it for pathogenic variants that compromise immune system integrity. The test identifies:

  • Point mutations affecting neutrophil chemotaxis and phagocytosis
  • Genetic alterations disrupting superoxide production in immune cells
  • Variants associated with impaired neutrophil extracellular trap formation
  • Mutations leading to abnormal actin cytoskeleton organization in white blood cells
  • Genetic markers for severe combined immunodeficiency manifestations

Clinical Indications: Who Should Consider This Test?

This specialized genetic test is recommended for individuals presenting with symptoms suggestive of neutrophil immunodeficiency disorders, including:

  • Recurrent bacterial, fungal, or viral infections requiring frequent hospitalization
  • Delayed wound healing and persistent skin infections
  • Autoimmune manifestations alongside immunodeficiency symptoms
  • Family history of immune system disorders or unexplained infant deaths
  • Abnormal neutrophil counts or function in laboratory assessments
  • Children with failure to thrive and recurrent opportunistic infections

Transformative Benefits of Genetic Testing

Undergoing the RAC2 Gene Neutrophil Immunodeficiency Syndrome NGS Genetic DNA Test provides numerous clinical advantages:

  • Precise Diagnosis: Eliminates diagnostic uncertainty and enables targeted treatment approaches
  • Family Planning Guidance: Provides crucial information for genetic counseling and reproductive decisions
  • Personalized Treatment: Facilitates development of customized therapeutic strategies based on genetic profile
  • Proactive Management: Allows for early intervention and preventive care measures
  • Comprehensive Care Coordination: Enables multidisciplinary approach involving immunologists, geneticists, and dermatologists

Understanding Your Genetic Test Results

Our comprehensive genetic analysis provides detailed insights into your immune system function:

  • Positive Result: Indicates presence of pathogenic RAC2 gene mutation, confirming neutrophil immunodeficiency syndrome diagnosis
  • Negative Result: Suggests absence of tested RAC2 mutations, though other genetic factors may require investigation
  • Variant of Uncertain Significance: Identifies genetic changes requiring additional clinical correlation and family studies
  • Carrier Status: Determines if individuals carry one copy of mutated gene without exhibiting symptoms

Test Specifications and Pricing

Test Component Details
Test Name RAC2 Gene Neutrophil Immunodeficiency Syndrome 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 Methodology Next-Generation Sequencing (NGS) Technology

Nationwide Accessibility and Comprehensive Support

We maintain diagnostic facilities across major metropolitan areas throughout the United States, ensuring convenient access to advanced genetic testing services. Our network includes specialized centers in New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Each location features state-of-the-art laboratory equipment and experienced genetic counselors who provide personalized guidance throughout the testing process.

Pre-Test Preparation Requirements

To ensure optimal testing accuracy and comprehensive analysis, we recommend:

  • Complete clinical history documentation of the patient undergoing testing
  • Genetic counseling session to construct detailed pedigree chart of family members affected by RAC2-related disorders
  • Review of previous immunological testing and treatment history
  • Coordination with referring physician for comprehensive clinical correlation

Take Control of Your Immune Health Today

Don’t let uncertainty about your immune system function compromise your quality of life. Our RAC2 Gene Neutrophil Immunodeficiency Syndrome NGS Genetic DNA Test provides the clarity needed for effective medical management and improved health outcomes. With our discounted price of $500 USD and comprehensive nationwide coverage, advanced genetic testing has never been more accessible.

Call our genetic specialists today at +1(267) 388-9828 to schedule your consultation and begin your journey toward precise diagnosis and personalized treatment. Our team is available to answer your questions, explain the testing process, and help you take the first step toward understanding your genetic health.