Find Answers for Unexplained Seizures and Movement Disorders
When your body experiences sudden seizures or involuntary movements without warning, it can feel like you’ve lost control of your own health. The uncertainty, the fear of when the next episode might strike, and the frustration of not knowing why – we understand how overwhelming this journey can be. Our KCNMA1 genetic test is designed to provide the clarity and answers you deserve, helping you and your healthcare team develop a targeted approach to managing your neurological health.
Understanding the KCNMA1 Genetic Test
The KCNMA1 gene plays a crucial role in regulating electrical activity in your brain and controlling muscle movements. When this gene doesn’t function properly, it can lead to two main conditions: generalized epilepsy (recurrent seizures affecting both sides of the brain) and paroxysmal dyskinesia (sudden, episodic involuntary movements). Our test uses Next Generation Sequencing (NGS) technology to examine your KCNMA1 gene with exceptional accuracy, identifying any variations that might be contributing to your symptoms.
Think of this test as a roadmap to understanding your body’s unique neurological wiring. Rather than guessing or treating symptoms blindly, you’ll have concrete genetic information that can guide your treatment decisions and help you understand your condition better.
Who Should Consider This Test?
This test may be right for you if you experience:
- Unexplained seizures that affect your entire body
- Sudden, episodic involuntary movements or muscle spasms
- A family history of epilepsy or movement disorders
- Neurological symptoms that haven’t responded to standard treatments
- Concerns about passing genetic conditions to your children
- Multiple neurological symptoms without clear diagnosis
Many South Africans live with these symptoms for years without understanding their cause. You don’t have to continue living with uncertainty – genetic testing can provide the answers that transform your approach to treatment and management.
Why This Test Matters for Your Health
Getting a genetic diagnosis can be life-changing for several reasons:
- Personalised Treatment: Knowing your specific genetic variant can help your neurologist choose medications that are more likely to be effective
- Family Planning: Understand the risk of passing the condition to your children and make informed decisions
- Peace of Mind: End the diagnostic odyssey and finally have answers about your condition
- Better Management: Develop targeted strategies to manage and potentially reduce episodes
- Early Intervention: For family members who might be at risk but haven’t developed symptoms yet
Many patients tell us that getting their genetic results felt like a weight had been lifted – they finally understood why their body was behaving this way and could move forward with confidence.
Understanding Your Results
We know that waiting for genetic test results can be anxiety-provoking. Here’s what to expect:
Positive Result: If we identify a variation in your KCNMA1 gene, this doesn’t mean your condition will worsen. It means we’ve found the underlying cause, which is the first step toward more effective management. Our genetic counsellor will explain exactly what the variation means for your health and treatment options.
Negative Result: If no KCNMA1 variations are found, this is valuable information too. It means your symptoms might be caused by other factors, and your doctor can explore alternative diagnostic paths with greater confidence.
Uncertain Result: Sometimes we find variations whose significance isn’t fully understood yet. In these cases, we’ll provide clear guidance about what this means and recommend next steps for monitoring or additional testing.
Remember: No matter your results, you’ll have the support of our genetic counselling team to help you understand and process the information.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price |
|---|---|---|
| KCNMA1 Genetic Test | ZAR 6,700 | |
| Genetic Counselling Session | INCLUDED | |
| NGS Technology Analysis | INCLUDED | |
| Results Interpretation | INCLUDED | |
Consider the value: This single test could save you years of unnecessary doctor visits, ineffective medications, and the emotional toll of not knowing what’s causing your symptoms.
What to Expect During Testing
Sample Collection: Simple blood draw or blood spot on FTA card – quick and virtually painless
Preparation: We’ll help you gather your clinical history and create a family pedigree chart during your genetic counselling session
Turnaround Time: 3-4 weeks for comprehensive results
Method: Advanced NGS (Next Generation Sequencing) technology for maximum accuracy
Why Trust Oracle Genomics?
Nationwide Coverage: We serve patients across South Africa, with convenient testing options in Johannesburg, Cape Town, Durban, Pretoria and throughout the country
Medical Expertise: Our tests are designed in consultation with neurologists and genetic specialists
Accuracy Guarantee: We use the latest NGS technology to ensure reliable, accurate results you can trust
Patient Support: From your first enquiry through to understanding your results, we’re here to support you every step of the way
Confidentiality: Your genetic information is handled with the utmost privacy and security
Take the First Step Toward Clarity Today
Don’t let uncertainty about your neurological health control your life any longer. Every day you wait is another day without answers that could transform your treatment and quality of life.
Book your test now and receive:
- Comprehensive KCNMA1 genetic analysis
- Professional genetic counselling session
- Clear, understandable results in 3-4 weeks
- Peace of mind and a path forward
Limited time special pricing – secure your test at ZAR 6,700 before the price increases to ZAR 9,350
You’re not alone in this journey. Thousands of South Africans have found answers through genetic testing. Take that first brave step today toward understanding your body and reclaiming control of your neurological health.
