Find Clarity About Hereditary Neuropathy with Our KIF1B Gene CMT2A1 DNA Test
Living with unexplained muscle weakness, numbness, or tingling in your hands and feet can be frightening and isolating. When these symptoms run in your family, the uncertainty can feel overwhelming. Our KIF1B Gene CMT2A1 NGS Genetic DNA Test provides the definitive answers you need to understand your genetic risk for Charcot-Marie-Tooth disease type 2A1, giving you the clarity to make informed decisions about your health and future.
Understanding Your KIF1B Gene CMT2A1 Test
The KIF1B gene plays a crucial role in nerve function, and mutations in this gene can lead to CMT2A1 – a specific form of Charcot-Marie-Tooth disease that affects the peripheral nerves. Our advanced Next Generation Sequencing (NGS) technology examines your DNA with exceptional accuracy, identifying even the smallest genetic variations that could indicate CMT2A1. This isn’t just a test – it’s a comprehensive genetic investigation that provides definitive answers about your neurological health.
Who Should Consider This Test?
This test is essential if you’re experiencing:
- Progressive muscle weakness in your feet, legs, hands, or arms
- Numbness, tingling, or burning sensations in your extremities
- Difficulty with balance or frequent tripping
- High arches in your feet or hammer toes
- Reduced sensation to touch, temperature, or pain
- A family history of similar neurological symptoms
If these symptoms sound familiar, or if CMT2A1 runs in your family, this test can provide the clarity you’ve been seeking.
Why Early Detection Matters for Your Health
Getting tested for KIF1B gene mutations offers profound benefits for your health journey:
- Peace of Mind: End the uncertainty and anxiety about your symptoms
- Early Intervention: Access appropriate treatments and management strategies sooner
- Family Planning: Make informed decisions about having children
- Personalised Care: Receive targeted neurological care based on your genetic profile
- Proactive Management: Implement lifestyle changes to preserve mobility and function
Understanding Your Test Results
We understand that waiting for genetic test results can be anxiety-provoking. Our process is designed to provide clarity and support:
- Comprehensive Analysis: Our neurological specialists carefully interpret your results
- Clear Explanation: You’ll receive easy-to-understand information about what your results mean
- Genetic Counselling: Professional guidance to help you understand implications for you and your family
- Next Steps: Clear recommendations for management and follow-up care
- Ongoing Support: Access to resources and specialists for continued care
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| KIF1B Gene CMT2A1 NGS Genetic DNA Test | ZAR 6,700 | ZAR 2,650 |
Price includes genetic counselling session, comprehensive analysis, and detailed results interpretation
Why Trust Oracle Genomics?
We’re committed to providing South Africans with accessible, reliable genetic testing:
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Neurological Specialists: Our team includes experienced neurologists and genetic counsellors
- Advanced NGS Technology: State-of-the-art testing for maximum accuracy
- 3-4 Week Turnaround: Quick results without compromising quality
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Comprehensive Preparation: Includes clinical history review and pedigree analysis
Take the First Step Toward Clarity Today
Don’t let uncertainty about your neurological health control your life. Our KIF1B Gene CMT2A1 test provides the answers you need to take control of your health journey. With our special pricing of ZAR 6,700 and comprehensive genetic counselling included, there’s never been a better time to get the clarity you deserve.
Limited Time Special: Book your test today and save ZAR 2,650 off the regular price. Your journey to neurological clarity starts with one simple decision.
