Find Answers for Unexplained Balance and Coordination Issues
When your body suddenly betrays you with episodes of unsteadiness, dizziness, or coordination problems, it can feel frightening and isolating. You’re not alone in this journey, and now you don’t have to face these mysterious symptoms without answers. Our episodic ataxia genetic test provides the clarity and understanding you’ve been searching for.
Understanding Your Episodic Ataxia Genetic Test
This advanced genetic test uses next-generation sequencing technology to examine 10 specific genes known to be associated with episodic ataxia. Think of it as reading your body’s genetic blueprint to identify potential variations that might be causing your symptoms. The test analyses genes including CACNA1A, CACNB4, KCNA1, and several others that play crucial roles in nerve cell communication and coordination.
Unlike basic neurological exams, this test provides molecular-level insights that can confirm or rule out genetic causes of your symptoms, giving you and your healthcare provider definitive information to guide your treatment plan.
Who Should Consider This Test?
This test is particularly important if you experience:
- Recurrent episodes of poor coordination or balance problems
- Sudden dizziness or vertigo that comes and goes
- Difficulty with fine motor skills during episodes
- Family history of similar neurological symptoms
- Unexplained slurred speech or eye movement issues
- Symptoms that worsen with stress, exercise, or fatigue
Many South Africans live with these symptoms for years without understanding their cause. Getting tested could be the first step toward effective management and improved quality of life.
Why Early Detection Matters for Your Health
Understanding the genetic basis of your symptoms provides numerous life-changing benefits:
- Accurate Diagnosis: Move from uncertainty to clarity about your condition
- Personalised Treatment: Receive targeted therapies rather than trial-and-error approaches
- Family Planning Insights: Understand inheritance patterns for future generations
- Symptom Management: Learn specific triggers and prevention strategies
- Peace of Mind: Reduce the anxiety of not knowing what’s causing your symptoms
Early genetic identification can help prevent years of unnecessary suffering and misdiagnosis.
Understanding Your Test Results
We understand that waiting for genetic test results can create anxiety. Here’s what to expect:
Your results will be carefully analysed by our expert neurologists and genetic specialists. You’ll receive a comprehensive report that clearly explains any genetic variations found and what they mean for your health. If variations are detected, we provide detailed information about:
- Specific gene mutations identified
- How these might affect your symptoms
- Recommended next steps and treatments
- Lifestyle modifications that could help
- When to follow up with your healthcare provider
Remember, having a genetic variation doesn’t necessarily mean you’ll develop severe symptoms – many factors influence how genes express themselves.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price |
|---|---|---|
| Episodic Ataxia Genetic Test | ZAR 8,700 | ZAR 7,800 |
| Includes comprehensive analysis of 10 genes, expert interpretation, and detailed report | ||
Consider this investment in your health: getting the right diagnosis early can save you thousands in unnecessary treatments and consultations over the years.
Why Trust Oracle Genomics?
- Nationwide Coverage: Convenient testing locations across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Expert Interpretation: All results reviewed by qualified neurologists and genetic specialists
- Advanced Technology: Using cutting-edge next-generation sequencing for maximum accuracy
- Fast Turnaround: Samples processed daily by 9 AM, with results in approximately 40 working days
- Patient-Focused Care: We understand the emotional journey of genetic testing and provide compassionate support
Take the First Step Toward Clarity Today
Don’t let unexplained symptoms control your life any longer. With our special pricing of ZAR 7,800, there’s never been a better time to get the answers you deserve.
Ready to book your test? Contact us today to schedule your appointment at a location convenient for you. Our team is ready to guide you through the simple process and answer any questions you might have.
Note: This test requires a duly filled Whole Exome Sequencing Consent Form (Form 37). We’ll help you complete this during your appointment.
Test Specifications
- Sample Required: 10 mL whole blood from 2 Lavender Top (EDTA) tubes
- Turnaround Time: Sample daily by 9 AM; Report in 40 working days
- Methodology: NGS with Sanger sequencing confirmation
- Genes Analysed: CACNA1A, CACNB4, GABRD, GABRG2, KCNA1, SCN1A, SCN1B, SCN2A, SCN9A, SLC1A3
- Specialty: Neurology
