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IgVH Mutation Detection Screening Test

Original price was: $376.Current price is: $250.

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The IgVH Mutation Detection Screening Test is a crucial molecular diagnostic tool used to detect mutations in the immunoglobulin heavy chain variable region genes. This test plays a vital role in diagnosing and prognosticating chronic lymphocytic leukemia (CLL), helping determine disease progression and treatment strategies. By analyzing the mutation status of IgVH genes, healthcare providers can identify patients with better or worse prognosis, enabling personalized treatment approaches. The test is performed using advanced PCR and sequencing technologies on blood samples, requiring no special preparation. Available for $250 USD (discounted from $376), this screening provides valuable insights for hematologists and oncologists managing leukemia patients. Results are typically available within a week, with samples processed on Mondays and reports delivered by Friday.

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IgVH Mutation Detection Screening Test

Understanding the IgVH Mutation Detection Screening Test

The IgVH Mutation Detection Screening Test represents a cutting-edge molecular diagnostic approach that examines the immunoglobulin heavy chain variable region genes in B-cells. This sophisticated test has revolutionized the management of chronic lymphocytic leukemia (CLL) by providing crucial prognostic information that directly impacts treatment decisions and patient outcomes.

Immunoglobulin heavy chain variable region genes play a fundamental role in the normal immune response, but when mutations occur in these genes within malignant B-cells, they can significantly influence disease behavior and progression. The presence or absence of these mutations serves as a powerful biomarker for predicting clinical outcomes in CLL patients.

What Does the Test Measure and Detect?

The IgVH Mutation Detection Screening Test specifically analyzes:

  • Mutation status of immunoglobulin heavy chain variable region genes
  • Somatic hypermutation patterns in B-cell receptors
  • Genetic variations that indicate disease prognosis
  • Molecular markers for treatment response prediction

This advanced molecular analysis utilizes polymerase chain reaction (PCR) and sequencing technologies to examine the DNA sequences of IgVH genes, identifying whether the malignant B-cells have undergone somatic hypermutation. The test distinguishes between mutated IgVH (associated with better prognosis) and unmutated IgVH (associated with more aggressive disease).

Who Should Consider This Test?

Clinical Indications and Symptoms

This screening test is recommended for individuals experiencing:

  • Unexplained lymphocytosis or elevated lymphocyte counts
  • Enlarged lymph nodes without apparent infection
  • Fatigue, weakness, or unexplained weight loss
  • Night sweats or recurrent infections
  • Abnormal blood counts suggesting hematological disorders

The test is particularly crucial for patients diagnosed with or suspected of having chronic lymphocytic leukemia. Hematologists and oncologists frequently order this test to establish prognosis and guide treatment decisions for CLL patients.

Benefits of Taking the IgVH Mutation Detection Test

Undergoing this comprehensive screening offers numerous advantages:

  • Accurate Prognosis Assessment: Provides reliable information about disease progression and survival expectations
  • Personalized Treatment Planning: Helps determine whether immediate treatment or watchful waiting is appropriate
  • Early Intervention Guidance: Identifies patients who may benefit from earlier, more aggressive therapy
  • Treatment Response Prediction: Assists in selecting the most effective therapeutic approaches
  • Comprehensive Disease Monitoring: Serves as a baseline for tracking disease evolution over time

Understanding Your Test Results

Your IgVH Mutation Detection Screening Test results will fall into one of two primary categories:

Mutated IgVH Status

Patients with mutated IgVH genes typically experience:

  • More indolent disease course
  • Longer treatment-free intervals
  • Better overall survival rates
  • May qualify for watchful waiting approaches

Unmutated IgVH Status

Patients with unmutated IgVH genes generally have:

  • More aggressive disease progression
  • Shorter time to first treatment
  • May require earlier therapeutic intervention
  • Potential need for more intensive treatment regimens

It’s essential to discuss your specific results with your hematologist or oncologist, who can provide personalized interpretation and treatment recommendations based on your complete clinical picture.

Test Information and Pricing

Test Component Details
Test Name IgVH Mutation Detection Screening Test
Discount Price $250 USD
Regular Price $376 USD
Turnaround Time Sample Monday by 9 AM; Report Friday
Sample Type 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube
Sample Handling Ship refrigerated. DO NOT FREEZE
Preparation No special preparation required

Nationwide Availability and Booking

We have diagnostic centers conveniently located across the United States, serving patients in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more cities nationwide.

Our state-of-the-art molecular diagnostics laboratories ensure accurate, reliable results using the latest PCR and sequencing technologies. Our experienced team of laboratory professionals and genetic specialists maintain the highest standards of quality and precision.

Take Control of Your Health Today

Don’t wait to get the critical information you need for proper leukemia management. The IgVH Mutation Detection Screening Test provides essential prognostic data that can significantly impact your treatment journey and long-term outcomes.

Ready to schedule your test? Contact us now:
Phone: +1(267) 388-9828
WhatsApp: +1(267) 388-9828

Our knowledgeable staff is available to answer your questions, help you understand the testing process, and schedule your appointment at a location convenient for you. Take the first step toward personalized leukemia care and informed treatment decisions.