Find Answers for Unexplained Neurological Symptoms
Living with unexplained numbness, tingling sensations, or muscle weakness can be frightening and isolating. When traditional tests don’t provide clear answers, our advanced genetic testing for Charcot-Marie-Tooth Disease and Sensory Neuropathies offers the clarity you deserve. We understand the anxiety that comes with neurological symptoms, and we’re here to provide the definitive answers that can guide your treatment journey.
Understanding Your Genetic Neurological Health
Charcot-Marie-Tooth disease represents a group of inherited disorders that damage peripheral nerves – the nerves outside your brain and spinal cord. Our Next Generation Sequencing technology examines over 90 specific genes associated with these conditions, providing a comprehensive analysis that traditional testing methods might miss. This isn’t just another test; it’s a roadmap to understanding your unique neurological makeup.
Are These Symptoms Familiar to You?
- Progressive muscle weakness in feet, ankles, legs, or hands
- Numbness or tingling sensations in extremities
- Difficulty with balance and coordination
- Foot deformities like high arches or hammertoes
- Decreased sensation to heat, cold, or touch
- Family history of similar neurological symptoms
- Unexplained tripping or falling
If you recognize these patterns in yourself or family members, genetic testing could provide the answers that have been eluding you.
Why Early Detection Matters for Your Neurological Health
Getting an accurate diagnosis isn’t just about putting a name to your symptoms – it’s about taking control of your health journey. With a clear genetic diagnosis, you and your healthcare team can:
- Develop targeted treatment and management strategies
- Understand disease progression and plan accordingly
- Make informed family planning decisions
- Connect with appropriate specialists and support networks
- Reduce the stress of uncertainty and multiple doctor visits
Understanding Your Results with Compassion
We know that waiting for genetic results can be anxiety-provoking. That’s why we provide clear, comprehensive reports that your neurologist can easily interpret. Our genetic counsellors are available to help you understand what your results mean for your health and your family. Whether the results confirm a diagnosis or rule out certain conditions, you’ll have the information needed to move forward with confidence.
Transparent Pricing – No Hidden Costs
| Test Option | Price | Savings |
|---|---|---|
| Special Price | ZAR 7,800 | ZAR 900 savings |
| Regular Price | ZAR 8,700 | – |
Consider this investment in your health: early detection can prevent years of unnecessary treatments and provide peace of mind that’s truly priceless.
Why South Africans Trust Oracle Genomics
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Developed in consultation with leading neurologists and genetic specialists
- Advanced Technology: Next Generation Sequencing provides superior accuracy over traditional methods
- Fast Turnaround: Results typically within 40 working days from sample receipt
- Patient-Focused: We understand the emotional journey of neurological testing
Take the First Step Toward Clarity Today
Don’t let uncertainty about your neurological symptoms control your life. Our genetic testing provides the answers that can transform your health journey. With convenient locations across South Africa and compassionate support throughout the process, there’s no reason to wait.
Remember: Early detection of inherited neuropathies can significantly improve quality of life and treatment outcomes. Your journey to understanding starts with one simple blood test.
Limited Time Special Price: Book now to secure your ZAR 7,800 pricing before this offer ends. Take control of your neurological health today.
Test Specifications:
- Sample Required: 10 mL whole blood from 2 Lavender Top (EDTA) tubes
- Turnaround Time: 40 working days
- Methodology: Next Generation Sequencing with Sanger confirmation
- Mandatory: Duly filled Whole Exome Sequencing Consent Form (Form 37)
- Specialty: Neurology
