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MED25 Gene CMT2B2 Genetic Test

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

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The MED25 Gene CMT2B2 NGS Genetic DNA Test is a cutting-edge genetic analysis designed to detect mutations in the MED25 gene associated with Charcot-Marie-Tooth disease type 2B2 (CMT2B2). This comprehensive next-generation sequencing test provides crucial diagnostic information for individuals experiencing peripheral neuropathy symptoms, muscle weakness, and sensory loss. By identifying specific genetic variants, the test enables accurate diagnosis, personalized treatment planning, and informed family counseling. The test costs $500 USD and offers valuable insights for patients with suspected inherited neurological disorders, helping guide appropriate medical management and therapeutic interventions.

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MED25 Gene CMT2B2 NGS Genetic DNA Test

Comprehensive Genetic Testing for Charcot-Marie-Tooth Disease Type 2B2

The MED25 Gene CMT2B2 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise detection of mutations associated with Charcot-Marie-Tooth disease type 2B2. This advanced next-generation sequencing technology provides comprehensive analysis of the MED25 gene, enabling accurate diagnosis and personalized treatment strategies for patients with inherited peripheral neuropathies.

What Does the MED25 Gene CMT2B2 Test Measure?

This sophisticated genetic test specifically targets the MED25 gene, which plays a critical role in neuronal function and peripheral nerve health. The test utilizes next-generation sequencing technology to:

  • Identify pathogenic variants in the MED25 gene
  • Detect single nucleotide polymorphisms (SNPs) associated with CMT2B2
  • Analyze gene copy number variations
  • Screen for novel mutations affecting neuronal function
  • Provide comprehensive genetic profiling for inherited neuropathies

Who Should Consider This Genetic Test?

The MED25 Gene CMT2B2 NGS Genetic DNA Test is recommended for individuals experiencing:

  • Progressive muscle weakness in hands and feet
  • Sensory loss or numbness in extremities
  • Foot deformities such as high arches or hammertoes
  • Difficulty walking or frequent tripping
  • Family history of peripheral neuropathy
  • Unexplained neurological symptoms in childhood or adulthood
  • Suspected inherited neurological disorders

Key Benefits of MED25 Genetic Testing

Undergoing the MED25 Gene CMT2B2 NGS Genetic DNA Test provides numerous advantages:

  • Accurate Diagnosis: Confirms or rules out CMT2B2 with high precision
  • Personalized Treatment: Guides targeted therapeutic interventions
  • Family Planning: Provides crucial information for genetic counseling
  • Early Intervention: Enables proactive management of symptoms
  • Disease Progression Monitoring: Helps track neurological changes over time
  • Research Contribution: Advances understanding of rare neurological conditions

Understanding Your Test Results

Your MED25 Gene CMT2B2 NGS Genetic DNA Test results will be carefully interpreted by our expert genetic counselors and neurologists:

  • Positive Result: Indicates the presence of MED25 gene mutations associated with CMT2B2, requiring comprehensive neurological evaluation and management
  • Negative Result: Suggests absence of tested MED25 mutations, though other genetic or acquired causes of neuropathy may need investigation
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact, requiring ongoing monitoring and potential family studies
  • Carrier Status: Determines if you carry mutations that could be passed to offspring

Test Pricing and Details

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

Pre-Test Requirements

Before undergoing the MED25 Gene CMT2B2 NGS Genetic DNA Test, patients must complete:

  • Comprehensive clinical history documentation
  • Genetic counseling session with certified genetic counselor
  • Development of detailed pedigree chart documenting family members affected with MED25-related conditions
  • Informed consent process explaining test implications and potential outcomes

Nationwide Testing Availability

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 other cities. Our network of certified genetic testing facilities ensures accessible, high-quality neurological genetic diagnostics for patients nationwide.

Take the Next Step Toward Neurological Health

Don’t let uncertainty about neurological symptoms affect your quality of life. The MED25 Gene CMT2B2 NGS Genetic DNA Test provides the clarity needed for proper diagnosis and management of inherited peripheral neuropathies. Our team of neurologists and genetic specialists is ready to guide you through the testing process and help interpret your results.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your MED25 genetic testing appointment and take control of your neurological health journey.