Understanding Your Neurological Health: LMNA Gene CMT2B1 DNA Testing
When you’re experiencing unexplained neurological symptoms or have a family history of nerve disorders, the uncertainty can be overwhelming. We understand the anxiety that comes with not knowing what’s causing your symptoms or whether you might pass on genetic conditions to your children. The LMNA Gene CMT2B1 NGS Genetic DNA Test provides the clarity you need to take control of your neurological health journey.
What This Test Detects
The LMNA Gene CMT2B1 test specifically looks for mutations in the LMNA gene that are associated with Charcot-Marie-Tooth disease type 2B1 (CMT2B1). This is an inherited neurological disorder that affects the peripheral nerves, leading to muscle weakness, sensory loss, and mobility challenges. Using advanced Next Generation Sequencing (NGS) technology, our test provides comprehensive analysis of your genetic makeup with exceptional accuracy.
Who Should Consider This Test?
This test is particularly important if you experience:
- Progressive muscle weakness in your feet, legs, or hands
- Difficulty with balance and coordination
- Reduced sensation in your extremities
- Foot deformities or high arches
- Family history of neurological disorders
- Concerns about passing genetic conditions to children
If you’re planning a family and have relatives with CMT or similar conditions, this test can provide valuable information for your reproductive decisions.
Why Early Detection Matters for Your Health
Getting tested for LMNA gene mutations offers significant benefits:
- Early Intervention: Identify genetic risks before severe symptoms develop
- Personalised Care: Work with neurologists to create targeted management plans
- Family Planning: Make informed decisions about having children
- Peace of Mind: Reduce uncertainty about your genetic health status
- Proactive Management: Implement lifestyle adjustments and monitoring strategies
Understanding Your Results
We know waiting for genetic test results can be stressful. Our team provides clear, compassionate explanations of your results, including:
- Detailed analysis of any detected mutations
- What your results mean for your neurological health
- Recommendations for next steps and specialist referrals
- Guidance on sharing results with family members
- Support resources for managing genetic conditions
Remember, a positive result doesn’t necessarily mean you’ll develop symptoms, but it empowers you with knowledge for proactive health management.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price |
|---|---|---|
| LMNA Gene CMT2B1 NGS Genetic DNA Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Consultation | Included | |
Consider this investment in your health: Early detection can prevent years of uncertainty and enable timely interventions that significantly improve quality of life.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Neurological Specialists: Working with qualified neurologists and genetic counsellors
- Advanced NGS Technology: State-of-the-art genetic sequencing for maximum accuracy
- Comprehensive Support: From initial counselling to results interpretation
- Proven Track Record: Trusted by healthcare professionals nationwide
Take the First Step Toward Clarity
Don’t let uncertainty about your neurological health hold you back. With results available in 3-4 weeks and convenient sample collection options (blood, extracted DNA, or simple blood spot on FTA card), getting tested has never been easier.
Limited Time Offer: Save ZAR 2,650 on your genetic testing while this special pricing lasts.
Convenient Locations: Testing available throughout South Africa with easy sample collection.
Your journey to neurological health clarity starts here. Contact Oracle Genomics today and take control of your genetic health story.
