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Ataxia Panel Genetic Test

Original price was: $750.Current price is: $500.

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The Ataxia Panel NGS Genetic DNA Test is a comprehensive genetic screening that utilizes Next Generation Sequencing technology to identify mutations associated with various forms of ataxia. This advanced diagnostic tool examines multiple genes simultaneously to detect inherited neurological disorders characterized by coordination problems, balance issues, and movement difficulties. The test is particularly valuable for individuals experiencing unexplained gait abnormalities, tremors, or speech difficulties. At just $500 USD, this panel provides crucial insights for diagnosis, treatment planning, and genetic counseling. Results typically take 3-4 weeks and require a simple blood sample or DNA extraction. Early detection through this test can significantly impact disease management and family planning decisions.

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Ataxia Panel NGS Genetic DNA Test

Comprehensive Genetic Testing for Neurological Coordination Disorders

The Ataxia Panel NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering comprehensive analysis of multiple genes associated with various forms of ataxia. Ataxia refers to a group of neurological disorders characterized by impaired coordination, balance problems, and movement difficulties resulting from damage to the cerebellum or its connections. This advanced testing panel utilizes cutting-edge Next Generation Sequencing (NGS) technology to provide detailed insights into the genetic underpinnings of these complex conditions.

What Does the Ataxia Panel Test Measure?

This comprehensive genetic panel examines numerous genes known to be associated with hereditary ataxias, including:

  • Spinocerebellar ataxia genes (SCA1, SCA2, SCA3, etc.)
  • Friedreich ataxia (FXN gene)
  • Ataxia-telangiectasia (ATM gene)
  • Episodic ataxia genes
  • Autosomal dominant and recessive ataxia genes
  • Mitochondrial ataxia-associated genes

The test identifies specific genetic mutations, deletions, duplications, and repeat expansions that contribute to the development of ataxia symptoms, providing crucial information for accurate diagnosis and personalized treatment approaches.

Who Should Consider This Genetic Test?

This test is recommended for individuals experiencing:

  • Unexplained coordination difficulties or balance problems
  • Progressive gait abnormalities
  • Speech difficulties or slurred speech
  • Involuntary eye movements (nystagmus)
  • Family history of neurological disorders
  • Early-onset movement disorders
  • Muscle weakness or tremors
  • Difficulty with fine motor skills

Key Benefits of Ataxia Panel Testing

  • Accurate Diagnosis: Provides definitive genetic confirmation of ataxia subtypes
  • Early Intervention: Enables timely treatment and management strategies
  • Family Planning: Offers crucial information for genetic counseling and reproductive decisions
  • Personalized Care: Guides targeted therapeutic approaches based on specific genetic findings
  • Prognostic Information: Helps predict disease progression and potential complications
  • Research Contribution: Advances understanding of neurological genetic disorders

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our team of neurological genetics specialists. Positive results indicate the presence of genetic mutations associated with ataxia, providing clear diagnostic information. Negative results suggest that no known genetic causes were identified in the tested genes, though clinical follow-up may still be recommended. Variants of uncertain significance may require additional family studies for clarification. All results include comprehensive genetic counseling to ensure proper understanding and appropriate next steps.

Test Pricing and Details

Test Feature Details
Test Name Ataxia Panel NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $750 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next Generation Sequencing (NGS) Technology

Pre-Test Requirements

Before undergoing the Ataxia Panel NGS Genetic DNA Test, patients should provide:

  • Complete clinical history documenting neurological symptoms
  • Participation in a genetic counseling session
  • Development of a detailed pedigree chart documenting family members affected with ataxia or related neurological conditions

Nationwide Testing Availability

We have convenient testing locations 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 the Next Step Toward Clarity

If you or a loved one are experiencing symptoms of ataxia or have a family history of neurological disorders, don’t wait to get answers. Our comprehensive Ataxia Panel NGS Genetic DNA Test provides the genetic insights needed for accurate diagnosis and effective management. Contact us today to schedule your test and begin your journey toward better neurological health.

Book Your Test Today: Call or WhatsApp +1(267) 388-9828

Our genetic specialists are available to answer your questions, provide detailed information about the testing process, and help you understand how genetic testing can benefit your specific situation. Take control of your neurological health with advanced genetic diagnostics from General Genetics Corporation.