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Common Neurological Neuromuscular Diseases Gene Panel

Original price was: $1,200.Current price is: $900.

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The Common Neurological Neuromuscular Diseases Gene Panel is a comprehensive genetic test that analyzes multiple genes associated with neurological and neuromuscular disorders. Using advanced Next-Generation Sequencing (NGS) technology, this panel detects genetic mutations responsible for conditions such as muscular dystrophy, amyotrophic lateral sclerosis (ALS), Charcot-Marie-Tooth disease, and various peripheral neuropathies. The test is particularly valuable for individuals experiencing unexplained muscle weakness, coordination difficulties, or family history of neurological conditions. Results provide crucial information for accurate diagnosis, treatment planning, and genetic counseling. The test costs $900 USD and requires a doctor’s prescription, with results available within 4-6 weeks. Sample collection involves amniotic fluid, chorionic villi, or peripheral blood using specialized collection containers.

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  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
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Common Neurological Neuromuscular Diseases Gene Panel

Comprehensive Genetic Testing for Neurological Disorders

The Common Neurological Neuromuscular Diseases Gene Panel represents a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to analyze multiple genes simultaneously associated with various neurological and neuromuscular conditions. This comprehensive genetic assessment provides crucial insights into inherited disorders affecting the nervous system, muscles, and peripheral nerves.

What This Advanced Genetic Panel Detects

Our sophisticated gene panel examines numerous genetic markers linked to:

  • Muscular dystrophies (Duchenne, Becker, and other forms)
  • Amyotrophic lateral sclerosis (ALS)
  • Charcot-Marie-Tooth disease and related neuropathies
  • Hereditary spastic paraplegias
  • Myasthenic syndromes
  • Peripheral neuropathies
  • Various inherited ataxias
  • Metabolic myopathies

Who Should Consider This Genetic Test?

Clinical Indications and Symptoms

This comprehensive genetic panel is recommended for individuals experiencing:

  • Unexplained progressive muscle weakness or wasting
  • Difficulty with coordination and balance
  • Muscle stiffness, cramps, or spasms
  • Family history of neurological or neuromuscular disorders
  • Delayed motor milestones in children
  • Progressive difficulty with walking or mobility
  • Sensory abnormalities including numbness or tingling
  • Unexplained fatigue or exercise intolerance

Significant Benefits of Genetic Testing

Why Choose Our Neurological Gene Panel?

  • Accurate Diagnosis: Provides definitive answers for complex neurological symptoms
  • Personalized Treatment: Enables targeted therapeutic approaches based on genetic findings
  • Family Planning: Offers valuable information for genetic counseling and reproductive decisions
  • Early Intervention: Facilitates timely management strategies for better outcomes
  • Comprehensive Analysis: Single test covering multiple potential genetic causes
  • Advanced Technology: Utilizes state-of-the-art NGS methodology for superior accuracy

Understanding Your Test Results

Interpreting Genetic Findings

Your results will be carefully analyzed and presented with comprehensive explanations:

  • Positive Results: Identification of pathogenic variants associated with specific neurological conditions
  • Negative Results: No disease-causing mutations detected in the analyzed genes
  • Variants of Uncertain Significance: Genetic changes with unclear clinical implications requiring further evaluation
  • Carrier Status: Information about recessive conditions that could affect future generations

All results include detailed interpretation by our genetic specialists and recommendations for next steps, including consultation with neurologists or genetic counselors.

Test Information and Pricing

Test Component Details
Test Name Common Neurological Neuromuscular Diseases Gene Panel
Discount Price $900 USD
Regular Price $1200 USD
Turnaround Time 4-6 weeks
Sample Type Amniotic fluid / Chorionic villi / Peripheral blood
Test Components Sterile container / Sterile Normal Saline Container / EDTA Vacutainer
Pre-test Requirements Doctor’s prescription required (not applicable for surgery, pregnancy, or travel abroad cases)

Nationwide Accessibility

We proudly serve patients across the United States with convenient testing locations in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified collection centers ensures accessible testing regardless of your location.

Take Control of Your Neurological Health

Don’t let unexplained neurological symptoms remain a mystery. Our comprehensive genetic panel provides the answers you need for proper diagnosis and effective treatment planning. With advanced NGS technology and expert genetic analysis, we deliver reliable results that can transform your healthcare journey.

Ready to uncover the genetic basis of your neurological concerns? Book your Common Neurological Neuromuscular Diseases Gene Panel today!

Call or WhatsApp us at +1(267) 388-9828 to schedule your test or speak with our genetic specialists about whether this comprehensive panel is right for you.

Take the first step toward understanding your neurological health with confidence and clarity.