Understanding Your Risk for Spinocerebellar Ataxia Type 5
If you’re worried about unexplained balance problems, coordination difficulties, or have family members affected by neurological conditions, you’re not alone. Many South Africans face the uncertainty of inherited disorders, and the SPTBN2 Gene Test provides the clarity you need to move forward with confidence.
What This Test Reveals About Your Health
The SPTBN2 Gene Test uses cutting-edge Next Generation Sequencing (NGS) technology to detect mutations in the SPTBN2 gene, which is responsible for Spinocerebellar Ataxia Type 5. This autosomal dominant condition means if one parent carries the gene, there’s a 50% chance of passing it to each child. Our test provides definitive answers about your genetic status, helping you understand your risk and plan accordingly.
Who Should Consider This Genetic Test?
- Individuals experiencing unexplained balance or coordination problems
- People with family history of Spinocerebellar Ataxia or similar neurological conditions
- Those planning pregnancy who want to understand genetic risks
- Individuals with symptoms like slurred speech, tremors, or difficulty walking
- Anyone seeking peace of mind about their neurological health
Why Early Detection Matters for Your Future
Knowing your genetic status empowers you to take proactive steps for your health. Early detection of SPTBN2 mutations allows for:
- Better management of potential symptoms through early intervention
- Informed family planning decisions
- Access to appropriate medical care and support services
- Reduced anxiety through definitive answers
- Opportunity to participate in clinical trials or research if needed
Understanding Your Test Results
Our genetic counsellors will walk you through your results with compassion and clarity. You’ll receive either:
- Negative Result: No SPTBN2 mutation detected – providing peace of mind for you and your family
- Positive Result: Mutation detected – connecting you with specialist neurologists and support resources
Regardless of the outcome, you’ll have a clear path forward with professional guidance every step of the way.
Transparent Pricing – Exceptional Value
| Test Feature | Details | Value |
|---|---|---|
| Regular Price | ZAR 9,350 | Comprehensive genetic analysis |
| Special Price | ZAR 6,700 | Limited time savings of ZAR 2,650 |
| Turnaround Time | 3-4 Weeks | Quick results for timely decisions |
| Sample Type | Blood or DNA sample | Simple, painless collection |
| Accuracy | 99.9% | Gold standard NGS technology |
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, and Pretoria
- Expert Guidance: Pre-test genetic counselling to understand your family history
- Medical Excellence: Collaboration with specialist neurologists
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Patient-Centred Care: Empathetic support throughout your journey
Take the First Step Toward Clarity Today
Don’t let uncertainty about your neurological health hold you back. With our special pricing of ZAR 6,700, now is the perfect time to get the answers you deserve. Our team is ready to support you with:
- Convenient booking options across major South African cities
- Professional genetic counselling sessions
- Clear, compassionate result explanations
- Ongoing support and specialist referrals if needed
Book your SPTBN2 Gene Test today and take control of your health future. Limited appointments available at this special price.
