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RAB7A Gene CMT2B Genetic Test

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

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The RAB7A Gene CMT2B NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the RAB7A gene associated with Charcot-Marie-Tooth disease type 2B (CMT2B). This comprehensive genetic analysis utilizes Next-Generation Sequencing (NGS) technology to provide precise detection of pathogenic variants that cause this inherited neurological disorder. The test is particularly valuable for individuals experiencing peripheral neuropathy symptoms, family members of diagnosed patients, and those with unexplained neurological symptoms. Results help guide treatment decisions, inform family planning, and provide clarity about disease progression. The test is available for $500 USD and provides results within 3-4 weeks using blood or extracted DNA samples. Genetic counseling is recommended before testing to ensure proper understanding of results and implications.

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RAB7A Gene CMT2B NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Disorders

The RAB7A Gene CMT2B NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise detection of mutations responsible for Charcot-Marie-Tooth disease type 2B. This advanced testing methodology provides crucial insights for patients and healthcare providers navigating complex neurological conditions.

What Does This Test Measure?

This specialized genetic test specifically targets the RAB7A gene, which plays a critical role in intracellular trafficking and neuronal function. Through Next-Generation Sequencing technology, the test identifies:

  • Pathogenic mutations in the RAB7A gene
  • Single nucleotide variants associated with CMT2B
  • Small insertions and deletions affecting gene function
  • Genetic markers indicating disease inheritance patterns

Who Should Consider This Test?

This genetic screening is particularly recommended for individuals experiencing:

  • Progressive weakness in feet and hands
  • Sensory loss in extremities
  • Foot deformities including high arches
  • Family history of peripheral neuropathy
  • Unexplained neurological symptoms
  • Previous inconclusive neurological evaluations

Clinical Benefits of Genetic Testing

Undergoing the RAB7A Gene CMT2B NGS Genetic DNA Test provides numerous advantages:

  • Accurate diagnosis confirmation
  • Personalized treatment planning
  • Family risk assessment and counseling
  • Early intervention opportunities
  • Improved disease management strategies
  • Enhanced quality of life through targeted care

Understanding Your Test Results

Our comprehensive genetic counseling services help interpret your results with clarity:

  • Positive Result: Indicates presence of RAB7A mutation; enables proactive management
  • Negative Result: Suggests alternative causes for symptoms; guides further investigation
  • Variant of Uncertain Significance: Requires additional family studies and clinical correlation

Test Pricing and Details

Test Component Price (USD)
Discount Price $500
Regular Price $700
Turnaround Time 3-4 Weeks
Sample Type Blood, Extracted DNA, or Blood on FTA Card

Nationwide Testing Availability

We proudly serve patients across the United States with convenient testing locations in all 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 neurological specialists ensures comprehensive care throughout your testing journey.

Take the Next Step Toward Clarity

Don’t let uncertainty about neurological symptoms affect your quality of life. Our expert team is ready to guide you through the genetic testing process with compassion and clinical excellence. Contact us today to schedule your RAB7A Gene CMT2B NGS Genetic DNA Test and begin your journey toward accurate diagnosis and effective management.

Call or WhatsApp: +1(267) 388-9828 to book your appointment or discuss your testing options with our genetic specialists.