Find Clarity for Your Neurological Health Concerns
When you’re experiencing unexplained muscle weakness, balance issues, or have watched family members struggle with similar symptoms, the uncertainty can be overwhelming. Our DYNC1H1 Gene Charcot-Marie-Tooth Disease Axonal Type 20 test provides the definitive answers you deserve, helping you take control of your neurological health journey.
Understanding the DYNC1H1 Gene Test
This advanced genetic test specifically examines the DYNC1H1 gene, which plays a crucial role in nerve function. When this gene has mutations, it can lead to Charcot-Marie-Tooth disease type 20 – a condition affecting the peripheral nerves that control movement and sensation in your arms and legs. Our Next-Generation Sequencing (NGS) technology provides the most accurate analysis available, giving you reliable results you can trust for making important health decisions.
Who Should Consider This Test?
This test is particularly important if you experience:
- Progressive muscle weakness in your feet, legs, or hands
- Foot deformities like high arches or hammertoes
- Difficulty with balance and coordination
- Reduced sensation in your extremities
- Family history of similar neurological symptoms
- Unexplained walking difficulties or frequent tripping
Many South Africans with these symptoms have found life-changing clarity through genetic testing, enabling them to pursue appropriate treatments and lifestyle adjustments.
Why Early Detection Matters for Your Health
Getting an accurate diagnosis through our DYNC1H1 test offers significant benefits:
- Peace of Mind: End the uncertainty about your symptoms
- Proactive Management: Early intervention can help slow disease progression
- Family Planning: Understand inheritance risks for future generations
- Targeted Treatment: Work with neurologists on appropriate therapies
- Lifestyle Adjustments: Make informed decisions about physical activities and daily life
Understanding Your Test Results
We know waiting for genetic test results can be anxiety-provoking. Our comprehensive approach includes:
- Clear Reporting: Easy-to-understand results with detailed explanations
- Genetic Counselling: Professional guidance to interpret your results
- Family Pedigree Analysis: Mapping your family history for complete context
- Neurologist Referral: Connection to specialists if needed
- Ongoing Support: Resources for managing your condition
Your results will clearly indicate whether DYNC1H1 gene mutations are present and what this means for your health management.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| DYNC1H1 Gene Test | ZAR 6,700 | ZAR 2,650 | |
| Genetic Counselling Session | INCLUDED | ||
| Family Pedigree Analysis | INCLUDED | ||
| Results Interpretation | INCLUDED | ||
Consider the long-term value: Early diagnosis can prevent costly complications and improve your quality of life significantly.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS methodology for maximum accuracy
- Quick Turnaround: Results typically available within 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Comprehensive Support: From initial consultation through results interpretation
Take the First Step Toward Clarity Today
Don’t let uncertainty about your neurological health continue to cause anxiety. Our special pricing of ZAR 6,700 makes this life-changing test more accessible than ever.
Limited Time Offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) won’t last forever. Secure your test today and take control of your neurological health journey.
“Getting the DYNC1H1 test gave me the answers I needed to properly manage my condition. The genetic counselling was incredibly helpful in understanding what the results meant for me and my family.” – Satisfied Patient, Cape Town
