Understanding Your Risk for Spinocerebellar Ataxia Type 1
When neurological symptoms begin to affect your coordination and movement, the uncertainty can be frightening. Spinocerebellar ataxia type 1 is an inherited condition that impacts the cerebellum, the part of your brain responsible for coordinating movement. If you have a family history of balance problems, coordination difficulties, or similar neurological symptoms, understanding your genetic risk can provide the clarity you need to plan for your future health.
What This Test Detects
The ATXN1 Gene Test specifically examines the genetic markers associated with spinocerebellar ataxia type 1, an autosomal dominant condition. This means that if one parent carries the affected gene, there’s a 50% chance their child will inherit the condition. Our advanced Next-Generation Sequencing (NGS) technology provides comprehensive analysis of the ATXN1 gene, identifying the specific genetic variations that cause this progressive neurological disorder.
Who Should Consider This Test
This test is particularly important if you experience:
- Progressive coordination and balance problems
- Family history of similar neurological symptoms
- Difficulty with speech articulation or swallowing
- Muscle stiffness or involuntary movements
- Planning for family and wanting to understand genetic risks
Why Early Detection Matters for Your Health
Knowing your genetic status provides significant advantages for managing your health journey. Early detection allows for:
- Proactive symptom management and treatment planning
- Informed family planning decisions
- Access to appropriate neurological care and support
- Reduced anxiety through certainty about your genetic status
- Opportunity to participate in clinical trials and research
Understanding Your Results
Our genetic counselling team will guide you through your results with compassion and expertise. We provide clear explanations about what your genetic findings mean for your health and your family. Whether your results show you carry the genetic variation or not, you’ll receive comprehensive guidance on next steps, monitoring recommendations, and available support resources.
Comprehensive Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| ATXN1 Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Considering the potential impact on your quality of life and future planning, this investment in your health provides invaluable peace of mind and actionable information.
Nationwide Coverage You Can Trust
Oracle Genomics brings expert neurological genetic testing to communities across South Africa. With convenient testing locations in Johannesburg, Cape Town, Durban, and Pretoria, accessing this crucial health information has never been easier. Our team of genetic specialists and neurologists ensure you receive the highest standard of care, from initial counselling through to results interpretation.
Take Control of Your Neurological Health Today
Don’t let uncertainty about hereditary conditions dictate your future. With our special pricing of ZAR 6,700, now is the time to gain the clarity you deserve. Our simple testing process requires only a blood sample or DNA extraction, with results available within 3-4 weeks.
Book your genetic counselling session today and take the first step toward understanding your genetic health. Early detection through the ATXN1 Gene Test could provide the information you need to make empowered decisions about your neurological wellbeing and family planning.
Contact Oracle Genomics now to schedule your appointment at a location convenient for you. Our compassionate team is ready to support you through every step of this important health journey.
