Find Clarity for Unexplained Neurological Symptoms
When muscle jerks, seizures, or coordination difficulties disrupt your life, finding answers becomes essential. Our SCARB2 Gene Epilepsy Test offers the clarity you need to understand progressive myoclonic epilepsy type 4 and its potential connection to kidney health. For South Africans seeking definitive genetic answers, this test provides peace of mind and a clear path forward.
Understanding Your SCARB2 Genetic Test
This advanced Next-Generation Sequencing (NGS) test examines the SCARB2 gene for mutations associated with progressive myoclonic epilepsy type 4. Unlike standard epilepsy tests, our comprehensive analysis specifically targets the genetic variations that can cause both neurological symptoms and potential kidney complications. The test requires only a simple blood sample or DNA extraction, making the process straightforward and accessible.
Who Should Consider This Genetic Test?
- Individuals experiencing unexplained muscle jerks or myoclonus
- Patients with progressive epilepsy symptoms that don’t respond to standard treatments
- Those with family history of epilepsy or neurological disorders
- Individuals showing both neurological symptoms and kidney function concerns
- Parents planning families who want to understand genetic risks
- Patients seeking definitive diagnosis after years of uncertainty
Why Early Detection Matters for Your Health
Identifying SCARB2 gene mutations early provides crucial advantages for managing your health journey. Early detection allows for:
- Targeted Treatment Approaches: Customise epilepsy management based on your specific genetic profile
- Proactive Kidney Monitoring: Implement preventive measures if renal involvement is indicated
- Informed Family Planning: Make confident decisions about starting a family
- Reduced Diagnostic Uncertainty: End years of searching for answers about your symptoms
- Personalised Care Planning: Work with neurologists to create a management strategy tailored to your genetic makeup
Understanding Your Test Results
Our genetic counselling team provides clear, compassionate guidance when explaining your results. We’ll help you understand:
- What specific SCARB2 gene variations mean for your health
- How results impact your epilepsy management approach
- Potential implications for kidney function monitoring
- Family inheritance patterns and risk assessment
- Next steps for ongoing care and specialist referrals
Remember: A positive result provides answers, not limitations. It empowers you with knowledge to manage your health proactively.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| SCARB2 Gene Epilepsy NGS Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Consider the long-term value: Early detection can prevent costly emergency treatments and provide years of better health management.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, and Pretoria
- Expert Neurological Focus: Specialised testing designed specifically for epilepsy and neurological conditions
- Advanced NGS Technology: State-of-the-art genetic sequencing for maximum accuracy
- Comprehensive Support: Genetic counselling included to ensure you understand your results fully
- Proven Accuracy: Reliable results you can trust for major health decisions
- South African Expertise: Understanding local healthcare needs and genetic diversity
Take the First Step Toward Clarity
Don’t let uncertainty about your neurological symptoms control your life. With results available in 3-4 weeks and comprehensive support throughout the process, now is the time to get the answers you deserve.
Limited Time Offer: Special pricing of ZAR 6,700 includes complete genetic counselling and family history analysis. Take advantage of this comprehensive package to get the clarity you need for your health journey.
“Knowledge is power when facing neurological conditions. Our SCARB2 test provides the definitive answers that can transform uncertainty into actionable health management.” – Oracle Genomics Neurology Specialist
