Understanding Your Neurological Health Concerns
When you notice changes in your coordination, balance, or movement, it can be deeply concerning. The uncertainty about what’s causing these symptoms can create significant anxiety for you and your family. Our TGM6 Gene Spinocerebellar Ataxia Type 35 test is designed to provide the clarity you need about potential genetic factors affecting your neurological health.
What This Test Detects
This advanced Next-Generation Sequencing (NGS) test specifically examines the TGM6 gene for mutations that cause Spinocerebellar Ataxia Type 35, an autosomal dominant condition. This means if one parent carries the mutation, there’s a 50% chance of passing it to each child. The test identifies specific genetic variations that affect the cerebellum – the part of your brain responsible for coordinating movement and balance.
Who Should Consider This Test
This test is particularly important if you experience:
- Unexplained balance problems or frequent stumbling
- Coordination difficulties affecting daily activities
- Family history of neurological or movement disorders
- Progressive speech changes or slurring
- Eye movement abnormalities
- Concerns about passing genetic conditions to children
Why Early Detection Matters for Your Health
Knowing your genetic status provides several crucial benefits:
- Early Intervention: Identify risks before significant symptoms develop
- Family Planning: Make informed decisions about having children
- Medical Management: Work with neurologists on appropriate care strategies
- Peace of Mind: Reduce uncertainty about your neurological health
- Proactive Health Planning: Prepare for potential future needs
Understanding Your Test Results
We understand that waiting for genetic test results can be stressful. Our team provides clear, compassionate explanations of your results:
- Positive Result: Indicates a TGM6 gene mutation is present. Our genetic counsellors will help you understand what this means and connect you with appropriate neurological specialists
- Negative Result: No mutation detected in the TGM6 gene, providing reassurance about this specific condition
- Uncertain Variant: Rare cases where a genetic change of unknown significance is found – we provide full guidance on next steps
Transparent Pricing and Value
| Service | Regular Price | Special Price |
|---|---|---|
| TGM6 Gene SCA35 NGS Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Considering the potential impact on your long-term health and quality of life, this investment in genetic clarity represents significant value compared to years of uncertainty and potential misdiagnosis.
Trust and Accessibility Across South Africa
Oracle Genomics brings world-class genetic testing to every corner of South Africa. With collection centres in Johannesburg, Cape Town, Durban, Pretoria, and nationwide, we ensure that advanced neurological genetic testing is accessible to all South Africans who need it.
Our commitment to accuracy is backed by:
- NGS technology for highest detection rates
- Experienced neurological genetics specialists
- Comprehensive pre-test genetic counselling
- Clear, patient-focused result explanations
- Ongoing support for your healthcare journey
Take Control of Your Neurological Health Today
Don’t let uncertainty about genetic risks affect your peace of mind. Early detection through our TGM6 Gene test can provide the answers you need to make informed health decisions.
Book your test now and take the first step toward genetic clarity:
- Call our genetic counselling team for personalised guidance
- Visit our website to find your nearest collection centre
- Schedule your appointment with confidence in our expertise
With results typically available within 3-4 weeks and comprehensive support throughout the process, Oracle Genomics makes advanced genetic testing a trusted, accessible resource for South African families concerned about neurological health.
