SYNE1 Gene Spinocerebellar Ataxia Type 8 Autosomal Recessive NGS Genetic DNA Test
Comprehensive Genetic Testing for Hereditary Neurological Disorders
The SYNE1 Gene Spinocerebellar Ataxia Type 8 Autosomal Recessive NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This advanced test specifically targets mutations in the SYNE1 gene, which plays a critical role in maintaining proper neurological function and coordination. Spinocerebellar ataxia type 8 is a progressive neurological condition characterized by impaired coordination, balance difficulties, and movement disorders that typically manifest in early adulthood.
What This Test Measures and Detects
Our comprehensive NGS genetic analysis examines the SYNE1 gene for specific mutations associated with autosomal recessive spinocerebellar ataxia type 8. The test identifies:
- Pathogenic variants in the SYNE1 gene sequence
- Autosomal recessive inheritance patterns
- Specific nucleotide changes affecting protein function
- Genetic markers for progressive neurological deterioration
- Risk assessment for family members
Who Should Consider This Genetic Test
This specialized genetic test is recommended for individuals experiencing:
- Progressive coordination difficulties and balance problems
- Family history of neurological disorders or ataxia
- Unexplained gait abnormalities or movement disorders
- Early-onset neurological symptoms without clear diagnosis
- Planning for family with known genetic risk factors
- Suspected hereditary neurological conditions
Key Benefits of SYNE1 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages:
- Accurate Diagnosis: Precise identification of SYNE1 gene mutations
- Early Intervention: Opportunity for proactive treatment planning
- Family Planning Guidance: Informed reproductive decisions
- Personalized Treatment: Tailored therapeutic approaches
- Genetic Counseling Support: Professional guidance for result interpretation
- Peace of Mind: Clear understanding of genetic status
Understanding Your Test Results
Our comprehensive genetic counseling team will help you interpret your results with clarity and compassion:
- Positive Result: Indicates presence of SYNE1 gene mutations associated with spinocerebellar ataxia type 8
- Negative Result: No detected mutations in the analyzed SYNE1 gene regions
- Variant of Uncertain Significance: Genetic changes requiring further clinical correlation
- Carrier Status: Identification of autosomal recessive carrier state
All results include detailed explanations and recommendations for next steps, including specialist referrals and management strategies.
Test Information and Pricing
| Test Component | Details |
|---|---|
| Test Name | SYNE1 Gene Spinocerebellar Ataxia Type 8 Autosomal Recessive 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 |
| Testing Method | Next-Generation Sequencing (NGS) Technology |
Nationwide Testing Availability
We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified genetic testing facilities ensures accessible, reliable testing nationwide.
Take Control of Your Neurological Health Today
Don’t let uncertainty about hereditary neurological conditions affect your quality of life. Our SYNE1 genetic test provides the clarity and information needed for informed healthcare decisions. With our discounted price of $500 USD, advanced genetic testing is more accessible than ever.
Ready to schedule your genetic test? Contact our genetic counseling specialists today at +1(267) 388-9828 or book your appointment online. Our team is available to answer your questions and guide you through the testing process with expertise and compassion.
