Find Clarity About Hereditary Neuropathy with Our CTDP1 Gene CMT4 DNA Test
Living with unexplained muscle weakness, numbness, or balance issues can be frightening and isolating. When neurological symptoms run in your family, the uncertainty can feel overwhelming. At Oracle Genomics, we understand the emotional journey you’re facing, and we’re here to provide the answers and support you deserve. Our CTDP1 Gene CMT4 NGS Genetic DNA Test offers precise, reliable detection of hereditary neuropathy conditions, giving you the clarity needed to make informed decisions about your health journey.
Understanding Your CTDP1 Gene CMT4 Test
This advanced genetic test specifically examines the CTDP1 gene using Next Generation Sequencing (NGS) technology, the gold standard in genetic testing. The CTDP1 gene plays a crucial role in nerve function, and mutations in this gene are associated with Charcot-Marie-Tooth disease type 4 (CMT4), a hereditary neurological condition affecting peripheral nerves. Our test doesn’t just provide results – it provides understanding. We break down complex genetic information into clear, actionable insights that you and your healthcare provider can use to develop the most effective management plan for your specific situation.
Who Should Consider This Test?
This test is particularly important if you’re experiencing:
- Progressive muscle weakness in feet, legs, hands, or arms
- Numbness or reduced sensation in extremities
- Difficulty with balance and coordination
- Foot deformities like high arches or hammertoes
- Family history of similar neurological symptoms
- Unexplained muscle atrophy or wasting
- Delayed motor development in children
If these symptoms sound familiar, or if neurological conditions run in your family, this test could provide the answers you’ve been seeking. Early detection means earlier intervention and better symptom management.
Why Early Detection Matters for Your Health
Getting tested for CTDP1 gene mutations offers significant benefits for your long-term health and quality of life:
- Peace of Mind: Either rule out hereditary conditions or confirm a diagnosis, ending years of uncertainty
- Proactive Management: Early detection allows for timely interventions, physical therapy, and lifestyle adjustments
- Family Planning: Understand inheritance patterns to make informed decisions about family planning
- Personalised Care: Work with your neurologist to develop a treatment plan tailored to your specific genetic profile
- Prevent Complications: Early intervention can help prevent or delay more severe symptoms and complications
Understanding Your Test Results
We know waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive support throughout the process. Your results will be clearly explained by our genetic counselling team, who will help you understand what the findings mean for your health and your family. Whether your results show a mutation or provide reassuring clarity, we’ll guide you through the next steps and connect you with appropriate specialists if needed. Remember, knowledge is power – understanding your genetic makeup empowers you to take control of your health journey.
Transparent Pricing & Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| CTDP1 Gene CMT4 NGS DNA Test | ZAR 6,700 | ZAR 2,650 |
Your investment includes: Advanced NGS testing technology, professional genetic counselling session, comprehensive results interpretation, and ongoing support from our medical team. Compared to the potential costs of undiagnosed neurological conditions, this test represents exceptional value for your long-term health.
Why Trust Oracle Genomics?
We’ve built our reputation on accuracy, compassion, and expertise:
- Nationwide Coverage: Accessible testing centres across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS technology ensuring 99.9% accuracy
- Comprehensive Support: Genetic counselling included with every test
- Fast Turnaround: Results typically within 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
Take the First Step Toward Clarity Today
Don’t let uncertainty about hereditary neuropathy control your life. Early detection through genetic testing can provide the answers you need to take proactive control of your health. Our team is ready to support you through every step of this journey with compassion and expertise.
Limited Time Special Pricing: Take advantage of our current special offer of ZAR 6,700 (regularly ZAR 9,350) and invest in your neurological health today. Your journey to clarity and peace of mind starts with one simple decision.
“Early detection transformed my family’s approach to neurological health. The clarity we gained was priceless.” – Satisfied Oracle Genomics Patient
