Understanding Your Neurological Health: TRPV4 Gene CMT2C Testing
If you’ve been experiencing unexplained muscle weakness, foot deformities, or have a family history of neurological conditions, you’re not alone. Many South Africans face uncertainty about their neurological health, wondering if their symptoms are connected to hereditary conditions. Our TRPV4 Gene CMT2C NGS Genetic DNA Test provides the clarity you need to understand your genetic risks and take proactive steps toward better health management.
What Does This Test Detect?
The TRPV4 Gene CMT2C test specifically identifies mutations in the TRPV4 gene that cause Charcot-Marie-Tooth disease type 2C (CMT2C). This is an inherited neurological disorder that affects the peripheral nerves, leading to muscle weakness, sensory loss, and sometimes vocal cord paralysis. Using Next-Generation Sequencing (NGS) technology, we analyze your DNA with 99.9% accuracy to detect even the smallest genetic variations that could impact your neurological health.
Who Should Consider This Test?
This test is particularly important if you experience:
- Progressive muscle weakness in hands and feet
- High arches or hammertoes
- Reduced sensation in limbs
- Family history of neurological disorders
- Unexplained balance problems or frequent falls
- Vocal cord weakness or breathing difficulties
If you’re planning a family and have relatives with CMT or similar conditions, this test can provide crucial information for your reproductive decisions.
Why Early Detection Matters for Your Health
Getting tested for TRPV4 gene mutations offers significant benefits:
- Peace of Mind: Eliminate uncertainty about your neurological symptoms
- Proactive Management: Early detection allows for better symptom management and treatment planning
- Family Planning: Understand inheritance risks for future generations
- Accurate Diagnosis: Differentiate CMT2C from other neurological conditions
- Personalized Care: Work with neurologists to create targeted treatment strategies
Understanding Your Test Results
We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive support throughout the process. Your results will clearly indicate whether TRPV4 gene mutations were detected, and our genetic counsellors will explain what this means for your health. Whether your results are positive or negative, you’ll receive personalized guidance on next steps and management options.
Remember: A positive result doesn’t mean symptoms will definitely develop, and a negative result provides valuable reassurance about your genetic risks.
Transparent Pricing & Value
| Service | Regular Price | Special Price |
|---|---|---|
| TRPV4 Gene CMT2C NGS Test | ZAR 6,700 | |
| Genetic Counselling Session | INCLUDED | |
| Family Pedigree Analysis | INCLUDED | |
| Results Interpretation | INCLUDED | |
Turnaround time: 3-4 weeks | Sample: Blood, Extracted DNA, or FTA Card
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 technology for unparalleled accuracy
- Comprehensive Support: Genetic counselling included with every test
- Proven Track Record: Trusted by healthcare professionals nationwide
Take the First Step Toward Neurological Clarity
Don’t let uncertainty about your neurological health create unnecessary anxiety. With our special pricing of ZAR 6,700, now is the perfect time to gain the genetic insights you need for informed health decisions.
Limited Time Offer: Book before the end of the month to secure your ZAR 6,700 special price and receive priority processing.
