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MTMR2 Gene CMT4B1 Genetic Test

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

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The MTMR2 Gene CMT4B1 NGS Genetic DNA Test is a specialized diagnostic tool that identifies mutations in the MTMR2 gene associated with Charcot-Marie-Tooth disease type 4B1 (CMT4B1). This comprehensive next-generation sequencing test provides crucial information for patients experiencing progressive muscle weakness, sensory loss, and peripheral neuropathy symptoms. By detecting specific genetic variations, the test enables accurate diagnosis, facilitates proper treatment planning, and helps assess inheritance risks for family members. The test is particularly valuable for individuals with family history of neurological disorders or those showing early signs of peripheral nerve damage. Results are typically available within 3-4 weeks, and the test is priced at $500 USD with genetic counseling included.

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MTMR2 Gene CMT4B1 NGS Genetic DNA Test

Comprehensive Introduction to MTMR2 Genetic Testing

The MTMR2 Gene CMT4B1 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, specifically designed to identify mutations in the MTMR2 (Myotubularin-Related Protein 2) gene. This sophisticated test plays a crucial role in diagnosing Charcot-Marie-Tooth disease type 4B1 (CMT4B1), a rare inherited neurological disorder affecting peripheral nerves. The importance of this test lies in its ability to provide definitive genetic confirmation, enabling healthcare providers to establish accurate diagnoses and develop targeted management strategies for patients experiencing progressive neurological symptoms.

What the Test Measures and Detects

This advanced genetic test utilizes Next-Generation Sequencing (NGS) technology to comprehensively analyze the MTMR2 gene for pathogenic variants. The test specifically detects:

  • Point mutations, deletions, and insertions in the MTMR2 gene
  • Autosomal recessive inheritance patterns associated with CMT4B1
  • Genetic variations affecting myelin sheath formation in peripheral nerves
  • Mutations that disrupt normal nerve signal transmission
  • Specific genetic markers linked to progressive peripheral neuropathy

Who Should Consider This Test

This genetic test is recommended for individuals experiencing specific neurological symptoms or having relevant family history:

Symptoms and Clinical Indications

  • Progressive muscle weakness in hands, feet, and lower limbs
  • Sensory loss including reduced sensation to touch, temperature, and vibration
  • Foot deformities such as high arches (pes cavus) or hammertoes
  • Difficulty walking or frequent tripping
  • Reduced or absent deep tendon reflexes
  • Early-onset peripheral neuropathy symptoms
  • Family history of Charcot-Marie-Tooth disease or similar neurological conditions

Benefits of Taking the MTMR2 Genetic Test

Undergoing this comprehensive genetic analysis provides numerous advantages for patients and their families:

  • Accurate Diagnosis: Provides definitive confirmation of CMT4B1, eliminating diagnostic uncertainty
  • Early Intervention: Enables timely implementation of appropriate management strategies
  • Family Planning Guidance: Helps assess inheritance risks for future generations
  • Personalized Treatment: Facilitates development of targeted therapeutic approaches
  • Prognostic Information: Provides insights into disease progression and expected outcomes
  • Genetic Counseling: Supports informed decision-making for patients and families

Understanding Your Test Results

Interpreting MTMR2 genetic test results requires professional genetic counseling. Our specialists provide comprehensive guidance:

  • Positive Result: Indicates presence of pathogenic MTMR2 mutations confirming CMT4B1 diagnosis
  • Negative Result: Suggests absence of detectable MTMR2 mutations, though other genetic causes may need investigation
  • Variant of Uncertain Significance: Requires additional family studies and clinical correlation
  • Carrier Status: Identifies individuals who carry one copy of mutated gene without showing symptoms

All results are accompanied by detailed explanations and recommendations for next steps from our certified genetic counselors.

Test Pricing Information

Test Component Price (USD)
Discount Price $500
Regular Price $700

Nationwide Testing Availability

We proudly offer the MTMR2 Gene CMT4B1 NGS Genetic DNA Test across all major cities in the United States. Our state-of-the-art testing facilities are conveniently located in:

  • New York, NY
  • Los Angeles, CA
  • Chicago, IL
  • Houston, TX
  • Phoenix, AZ
  • Philadelphia, PA
  • San Antonio, TX
  • San Diego, CA
  • Dallas, TX
  • San Jose, CA

Additional testing centers are available throughout the country to ensure accessibility for all patients.

Book Your Genetic Test Today

Take the first step toward definitive neurological diagnosis and personalized care. Our genetic counseling team is ready to assist you with comprehensive pre-test guidance and post-result support. Contact us now to schedule your MTMR2 Gene CMT4B1 NGS Genetic DNA Test and begin your journey toward accurate diagnosis and effective management.

Call or WhatsApp: +1(267) 388-9828

Our genetic specialists are available to answer your questions, provide detailed test information, and help you understand the testing process from sample collection to result interpretation.