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COX20 Gene Ataxia and Muscle Hypotonia Genetic Test

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

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The COX20 Gene Ataxia and Muscle Hypotonia NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the COX20 gene associated with neurological disorders. This advanced next-generation sequencing test provides crucial diagnostic information for individuals experiencing coordination difficulties, muscle weakness, and movement disorders. The test helps confirm diagnoses, guide treatment strategies, and provide valuable information for family planning. Available for $500 USD, this specialized genetic test offers precise detection of COX20 gene variants that cause ataxia and muscle hypotonia, enabling early intervention and personalized care approaches for affected individuals and their families.

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COX20 Gene Ataxia and Muscle Hypotonia NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Disorders

The COX20 Gene Ataxia and Muscle Hypotonia NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise identification of mutations in the COX20 gene that are responsible for complex movement disorders. This specialized test utilizes cutting-edge next-generation sequencing technology to provide comprehensive analysis of genetic variations associated with ataxia and muscle weakness conditions.

What Does This Test Measure?

This advanced genetic test specifically targets the COX20 gene, which plays a critical role in mitochondrial function and energy production within nerve cells. The test detects:

  • Pathogenic mutations in the COX20 gene
  • Single nucleotide variants (SNVs) affecting protein function
  • Insertions and deletions that disrupt gene expression
  • Copy number variations impacting mitochondrial complex assembly

Who Should Consider This Test?

This genetic test is recommended for individuals experiencing:

  • Progressive coordination difficulties and balance problems
  • Muscle weakness and reduced muscle tone (hypotonia)
  • Difficulty with fine motor skills and coordination
  • Family history of neurological disorders
  • Unexplained movement disorders in childhood or adulthood
  • Developmental delays affecting motor function

Key Benefits of COX20 Genetic Testing

  • Accurate Diagnosis: Provides definitive identification of COX20 gene mutations
  • Early Intervention: Enables timely treatment and management strategies
  • Family Planning: Offers valuable information for genetic counseling
  • Personalized Care: Guides targeted therapeutic approaches
  • Prognostic Information: Helps predict disease progression and outcomes

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our expert genetic counselors and neurologists. Positive results indicating COX20 gene mutations confirm the genetic basis of your symptoms and provide essential information for developing a comprehensive management plan. Negative results help rule out this specific genetic cause, allowing your healthcare team to explore other potential diagnoses. All results come with detailed explanations and recommendations for next steps in your care journey.

Test Pricing Information

Price Type Amount (USD)
Discount Price $500
Regular Price $700

Nationwide Testing Availability

We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality testing standards nationwide.

Take Control of Your Neurological Health

Don’t let unexplained neurological symptoms control your life. The COX20 Gene Ataxia and Muscle Hypotonia NGS Genetic DNA Test provides the answers you need to move forward with confidence. Our team of genetic specialists and neurologists are ready to support you through every step of the testing process.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Take the first step toward understanding your genetic health and accessing personalized care solutions.