Understanding Your Neurological Health Concerns
Living with unexplained muscle weakness, numbness, or balance issues can be frightening and isolating. When these symptoms run in families, the uncertainty becomes even more overwhelming. The GJB1 Gene CMTX1 NGS Genetic DNA Test provides the clarity you need to understand hereditary peripheral nerve disorders, giving you and your family the power to make informed health decisions.
What This Test Detects
This advanced genetic test specifically identifies mutations in the GJB1 gene, which are responsible for Charcot-Marie-Tooth disease type X1 (CMTX1). CMTX1 is an inherited neurological condition that affects the peripheral nerves controlling muscle movement and sensation. Using Next-Generation Sequencing technology, we provide the most accurate detection available, ensuring you receive reliable results for this complex condition.
Who Should Consider This Test
This test is particularly important if you experience:
- Progressive muscle weakness in hands, feet, or legs
- Numbness or tingling sensations in extremities
- Difficulty with balance and coordination
- Foot deformities or high arches
- Family history of similar neurological symptoms
- Unexplained muscle wasting or atrophy
Why Early Detection Matters for Your Health
Understanding your genetic status provides numerous health benefits:
- Early Intervention: Allows for proactive management strategies before significant disability develops
- Family Planning: Provides crucial information for making informed reproductive decisions
- Treatment Guidance: Helps neurologists develop targeted management plans
- Peace of Mind: Reduces uncertainty and anxiety about your neurological health
- Prevention Planning: Enables lifestyle adjustments to minimize symptom progression
Understanding Your Results with Confidence
Our comprehensive approach includes professional genetic counselling to ensure you fully understand your results. We provide clear, compassionate explanations of what your genetic findings mean for your health and your family. Whether your results indicate a mutation or provide reassuring clarity, our medical team supports you through every step of the process with expert guidance and ongoing resources.
Transparent Pricing and Value
| Service | Regular Price | Special Price |
|---|---|---|
| GJB1 CMTX1 NGS Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included at no extra cost | |
| Family Pedigree Analysis | Comprehensive mapping included | |
| Results Interpretation | Expert neurological review included | |
Trusted Nationwide Coverage
Oracle Genomics provides accessible genetic testing across South Africa, with convenient sample collection available in Johannesburg, Cape Town, Durban, Pretoria, and nationwide. Our network of qualified healthcare professionals ensures you receive the same high standard of care regardless of your location.
Take Control of Your Neurological Health Today
Don’t let uncertainty about hereditary neuropathy control your life. With results in just 3-4 weeks and our special pricing of ZAR 6,700, there’s never been a better time to gain clarity about your genetic health. Our simple sample collection process (blood or DNA sample) makes testing convenient and stress-free.
Book your GJB1 CMTX1 genetic test now and take the first step toward understanding your neurological health with confidence. Contact Oracle Genomics today to schedule your genetic counselling session and begin your journey to clarity.
