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ATXN10 Gene Spinocerebellar Ataxia Type 10 Autosomal Dominant Genetic Test

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

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The ATXN10 Gene Spinocerebellar Ataxia Type 10 Autosomal Dominant NGS Genetic DNA Test is a comprehensive diagnostic tool designed to detect mutations in the ATXN10 gene associated with spinocerebellar ataxia type 10 (SCA10). This neurological disorder affects coordination, balance, and motor function through progressive degeneration of the cerebellum. Using Next-Generation Sequencing (NGS) technology, this test provides precise identification of expanded ATTCT pentanucleotide repeats in the ATXN10 gene, which are characteristic of SCA10. The test is particularly valuable for individuals experiencing unexplained coordination difficulties, balance problems, or those with family histories of ataxia disorders. Results typically take 3-4 weeks and require a simple blood sample or extracted DNA. At only $500 USD, this test offers crucial information for diagnosis, treatment planning, and genetic counseling for affected families.

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ATXN10 Gene Spinocerebellar Ataxia Type 10 Autosomal Dominant NGS Genetic DNA Test

Understanding Spinocerebellar Ataxia Type 10

Spinocerebellar ataxia type 10 (SCA10) represents a significant neurological disorder characterized by progressive degeneration of the cerebellum, the brain region responsible for coordinating movement and maintaining balance. This autosomal dominant condition results from specific genetic mutations in the ATXN10 gene, making genetic testing essential for accurate diagnosis and family planning.

What This Test Measures and Detects

Our advanced NGS Genetic DNA Test specifically targets the ATXN10 gene to identify expanded ATTCT pentanucleotide repeats, the hallmark genetic abnormality in SCA10. The test provides comprehensive analysis of:

  • ATTCT repeat expansion size and configuration
  • Genetic mutation patterns associated with SCA10
  • Inheritance risk assessment for family members
  • Disease progression prediction markers

Who Should Consider This Genetic Test

Symptoms and Clinical Indications

This test is recommended for individuals experiencing:

  • Progressive coordination difficulties and balance problems
  • Unsteady gait and frequent stumbling
  • Slurred speech and dysarthria
  • Involuntary eye movements (nystagmus)
  • Family history of ataxia or neurological disorders
  • Unexplained tremors or motor control issues

Benefits of ATXN10 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Accurate Diagnosis: Confirms or rules out SCA10 with high precision
  • Early Intervention: Enables timely treatment and management strategies
  • Family Planning: Provides crucial information for reproductive decisions
  • Prognostic Insights: Helps predict disease progression and severity
  • Personalized Care: Guides development of targeted treatment plans

Understanding Your Test Results

Our genetic counselors provide comprehensive interpretation of your results:

  • Normal Results: No expanded ATTCT repeats detected, indicating low SCA10 risk
  • Intermediate Alleles: Slightly expanded repeats requiring monitoring
  • Pathogenic Expansion: Confirmed SCA10 diagnosis with specific repeat size
  • Genetic Counseling: Detailed explanation of inheritance patterns and family implications

Test Pricing and Details

Test Feature Details
Test Name ATXN10 Gene Spinocerebellar Ataxia Type 10 Autosomal Dominant 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

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 network ensures accessible genetic testing services for patients nationwide.

Book Your Genetic Test Today

Take the first step toward understanding your neurological health. Our experienced genetic counselors and neurologists are ready to provide comprehensive testing and support. Contact us today to schedule your appointment and begin your journey to accurate diagnosis and personalized care.

Call or WhatsApp: +1(267) 388-9828

Our dedicated team will guide you through the testing process, answer your questions, and ensure you receive the highest quality genetic testing services available.

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