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HSPB8 Gene Neuronopathy Distal Hereditary Motor Type 2A Genetic Test

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

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The HSPB8 Gene Neuronopathy Distal Hereditary Motor Type 2A NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies mutations in the HSPB8 gene responsible for distal hereditary motor neuropathy type 2A. This comprehensive genetic analysis utilizes next-generation sequencing technology to detect specific genetic variations that cause progressive motor neuron degeneration affecting the peripheral nervous system. The test is essential for individuals experiencing muscle weakness, foot deformities, or family history of neurological disorders. Early detection enables proactive management strategies and informed family planning decisions. Our testing process includes pre-test genetic counseling to ensure comprehensive understanding of results and implications. Results are typically available within 3-4 weeks from sample collection. The test is available for $500 USD, providing accessible advanced genetic diagnostics for neurological conditions.

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HSPB8 Gene Neuronopathy Distal Hereditary Motor Type 2A NGS Genetic DNA Test

Comprehensive Genetic Testing for Hereditary Motor Neuron Disorders

The HSPB8 Gene Neuronopathy Distal Hereditary Motor Type 2A NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise detection of mutations associated with distal hereditary motor neuropathy type 2A. This advanced testing methodology provides crucial insights for patients and families affected by progressive motor neuron degeneration, enabling early intervention and personalized treatment approaches.

What Does This Test Measure and Detect?

This sophisticated genetic analysis specifically targets the HSPB8 gene, which encodes heat shock protein beta-8, a critical protein involved in maintaining neuronal health and function. The test utilizes next-generation sequencing (NGS) technology to identify:

  • Pathogenic mutations in the HSPB8 gene associated with distal hereditary motor neuropathy type 2A
  • Specific genetic variants that disrupt normal protein function in motor neurons
  • Inheritance patterns and risk assessment for family members
  • Genetic markers that influence disease progression and severity

Who Should Consider This Genetic Test?

Clinical Indications and Symptoms

This test is recommended for individuals experiencing:

  • Progressive muscle weakness beginning in the feet and hands
  • Foot deformities such as pes cavus (high arches) or hammertoes
  • Difficulty with fine motor skills and coordination
  • Family history of similar neurological symptoms
  • Unexplained muscle atrophy or wasting
  • Sensory disturbances in the distal extremities
  • Early-onset motor symptoms before age 30

Benefits of HSPB8 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Early Diagnosis: Enables prompt identification of hereditary motor neuron disorders
  • Personalized Treatment: Guides targeted therapeutic interventions and management strategies
  • Family Planning: Provides crucial information for genetic counseling and reproductive decisions
  • Proactive Monitoring: Facilitates regular neurological assessments and preventive care
  • Clinical Trial Eligibility: Opens opportunities for participation in cutting-edge research studies
  • Psychological Relief: Reduces uncertainty and provides clarity about genetic status

Understanding Your Test Results

Our comprehensive genetic counseling ensures you fully understand your test outcomes:

  • Positive Result: Indicates the presence of HSPB8 gene mutations associated with distal hereditary motor neuropathy type 2A, requiring specialized neurological care and family screening
  • Negative Result: Suggests absence of known HSPB8 mutations, though continued monitoring may be recommended based on clinical presentation
  • Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications, requiring ongoing research and periodic re-evaluation
  • Carrier Status: Determines if you carry a single copy of the mutation, important for family planning considerations

Test Details and Pricing

Test Component Details
Test Name HSPB8 Gene Neuronopathy Distal Hereditary Motor Type 2A 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
Specialty Neurology
Department Genetics
Method NGS Technology
Disease Type Neurological Disorders

Nationwide Accessibility and Expert Care

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 Control of Your Neurological Health Today

Don’t let uncertainty about hereditary motor neuron disorders impact your quality of life. Our HSPB8 genetic testing provides the clarity and information needed to make informed healthcare decisions. With our discounted rate of $500 USD, advanced neurological genetic testing is more accessible than ever.

Ready to schedule your genetic test? Contact our dedicated team today:

Phone: +1(267) 388-9828

Our genetic specialists are available to discuss your concerns, answer questions about the testing process, and help you schedule an appointment at your convenience. Take the first step toward understanding your genetic health and securing your neurological future.