Understanding Your Genetic Risk for Hereditary Ataxia
When neurological symptoms appear or run in your family, the uncertainty can be overwhelming. Our ATXN7 Gene Spinocerebellar Ataxia Type 7 test provides the clarity you need to understand your genetic inheritance and make empowered health decisions. For families across South Africa facing the possibility of hereditary neurological conditions, this test offers definitive answers and peace of mind.
What This Test Reveals About Your Health
The ATXN7 gene test uses Next Generation Sequencing (NGS) technology to examine your DNA for mutations that cause Spinocerebellar Ataxia Type 7. This autosomal dominant condition means if one parent carries the gene mutation, there’s a 50% chance of passing it to each child. The test specifically looks for expanded CAG repeats in the ATXN7 gene, which are responsible for the progressive neurological symptoms characteristic of this condition.
Our advanced NGS technology provides comprehensive analysis with exceptional accuracy, giving you reliable results you can trust for making important health and family planning decisions.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Progressive coordination difficulties and balance problems
- Family history of ataxia or similar neurological conditions
- Vision changes, including retinal degeneration
- Difficulty with speech and swallowing
- Muscle weakness or involuntary movements
- Planning for pregnancy with family history of neurological disorders
If you’re noticing early symptoms or have concerns about hereditary conditions in your family, this test provides the answers needed for proper medical management and family planning.
Why Early Detection Matters for Your Neurological Health
Getting tested for ATXN7 gene mutations offers significant benefits for your health journey:
- Early Intervention: Identify genetic risk before severe symptoms develop
- Family Planning: Make informed decisions about having children
- Proper Diagnosis: Differentiate between various types of ataxia for targeted treatment
- Peace of Mind: Reduce uncertainty about your genetic inheritance
- Medical Management: Work with neurologists to develop appropriate care plans
- Clinical Trial Eligibility: Access emerging treatments and research opportunities
Early genetic testing can significantly impact your quality of life and healthcare outcomes.
Understanding Your Test Results with Compassion
We understand that genetic testing can create anxiety, which is why we provide comprehensive support throughout the process. Your results will clearly indicate:
- Normal Result: No ATXN7 gene mutation detected – significant relief and reduced worry
- Positive Result: ATXN7 mutation identified – enabling proactive health management
- Inconclusive Result: Rare cases requiring additional analysis – we guide you through next steps
Every positive result includes genetic counselling to help you understand the implications and connect you with appropriate neurological specialists. We’re here to support you regardless of the outcome.
Transparent Pricing – Exceptional Value for Your Health
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| ATXN7 Gene Test with Genetic Counselling | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
Your investment includes: Comprehensive NGS genetic analysis, genetic counselling session, detailed results interpretation, and ongoing support. Compared to potential lifelong medical costs of undiagnosed neurological conditions, this test represents exceptional value for your long-term health.
Why Thousands of South Africans Trust Oracle Genomics
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS sequencing for 99.9% accuracy
- Genetic Counselling: Professional guidance included with every test
- Rapid Turnaround: Results typically available within 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood drop
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about hereditary neurological conditions control your future. With our special pricing of ZAR 6,700 and comprehensive genetic counselling, there’s never been a better time to gain the answers you deserve.
Book your ATXN7 gene test now and receive:
- Definitive genetic answers about hereditary ataxia risk
- Professional genetic counselling session
- Clear, understandable results interpretation
- Access to neurological specialists if needed
- Peace of mind for you and your family
Contact us today to schedule your genetic counselling and testing. Our compassionate team is ready to help you navigate this important health decision with confidence and care.
Test Specifications
- Method: Next Generation Sequencing (NGS) Technology
- Turnaround Time: 3-4 Weeks
- Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
- Preparation: Clinical History and Genetic Counselling Session Required
- Medical Specialty: Neurological Genetics
