ATXN7 Gene Spinocerebellar Ataxia Type 7 Autosomal Dominant NGS Genetic DNA Test
Comprehensive Genetic Testing for Hereditary Neurological Disorders
The ATXN7 Gene Spinocerebellar Ataxia Type 7 Autosomal Dominant NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This advanced testing methodology utilizes Next Generation Sequencing (NGS) technology to provide precise detection of mutations in the ATXN7 gene, which is responsible for spinocerebellar ataxia type 7 – a progressive neurodegenerative disorder affecting coordination, vision, and motor function.
What This Test Measures and Detects
This sophisticated genetic analysis specifically targets the ATXN7 gene located on chromosome 3p14.1, identifying the characteristic CAG trinucleotide repeat expansions that define spinocerebellar ataxia type 7. The test provides comprehensive assessment of:
- CAG repeat expansion size in the ATXN7 gene
- Presence of pathogenic mutations associated with autosomal dominant inheritance
- Genetic variations that correlate with disease severity and progression
- Expansion patterns that help predict age of onset and clinical manifestations
Who Should Consider This Genetic Test
This specialized genetic testing is recommended for individuals experiencing:
- Progressive coordination difficulties and balance problems
- Family history of spinocerebellar ataxia or unexplained neurological disorders
- Vision changes including macular degeneration and retinal pigment changes
- Speech difficulties and swallowing problems of unknown origin
- Unexplained progressive neurological symptoms in multiple family members
- Individuals planning family with known ataxia risk factors
Clinical Benefits of ATXN7 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous clinical advantages:
- Accurate Diagnosis: Confirms or rules out spinocerebellar ataxia type 7 with high precision
- Early Intervention: Enables proactive management strategies before significant neurological decline
- Family Planning: Provides crucial information for reproductive decision-making
- Treatment Guidance: Helps neurologists develop targeted symptom management approaches
- Prognostic Information: Offers insights into potential disease progression and timeline
- Genetic Counseling: Supports informed decisions about testing for at-risk family members
Understanding Your Test Results
Your comprehensive test report will include detailed interpretation by our certified genetic counselors:
- Normal Results: No pathogenic ATXN7 mutations detected, indicating low risk for spinocerebellar ataxia type 7
- Positive Results: Identification of CAG repeat expansions confirming diagnosis, with specific repeat size information
- Intermediate Alleles: Results that may require additional family studies for complete interpretation
- Clinical Correlation: Detailed explanation of how genetic findings relate to symptoms and prognosis
Test Pricing and Service Details
| Service | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
| Turnaround Time | 3-4 Weeks |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card |
Nationwide Accessibility and Support
We maintain comprehensive testing facilities across the United States, with specialized centers in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures convenient access to advanced genetic testing services regardless of your location.
Take Control of Your Neurological Health
Don’t let uncertainty about hereditary neurological conditions affect your quality of life. Our ATXN7 Gene Spinocerebellar Ataxia Type 7 NGS Genetic DNA Test provides the clarity and confidence you need for informed healthcare decisions. With results available in just 3-4 weeks and comprehensive genetic counseling included, you’ll receive the expert guidance necessary to understand your genetic profile and plan for the future.
Ready to begin your genetic testing journey? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online to schedule your comprehensive ATXN7 genetic analysis.
