Understanding Your Genetic Risk for Hereditary Neuropathy
When you’re concerned about unexplained neurological symptoms or have a family history of muscle weakness and numbness, the uncertainty can feel overwhelming. Our SBF2 Gene CMT4B2 NGS Genetic DNA Test provides the answers you need to make informed decisions about your health journey. We understand that genetic testing can feel daunting, which is why we’ve created a supportive, professional environment where your concerns are heard and addressed with compassion.
What Does the SBF2 Gene Test Detect?
This advanced genetic test specifically examines the SBF2 gene for mutations associated with Charcot-Marie-Tooth disease type 4B2 (CMT4B2). Using Next Generation Sequencing (NGS) technology, we can identify even the smallest genetic variations that might be missed by traditional testing methods. CMT4B2 is a hereditary neuropathy that affects the peripheral nerves, leading to progressive muscle weakness and sensory loss, typically beginning in childhood or adolescence.
Who Should Consider This Genetic Test?
This test is particularly important if you experience:
- Unexplained muscle weakness in your hands, feet, or legs
- Progressive numbness or tingling sensations
- Difficulty with balance or coordination
- Foot deformities or high arches
- Family history of similar neurological symptoms
- Known CMT4B2 diagnosis in close relatives
Early detection through genetic testing can help you and your healthcare team develop proactive management strategies and connect with appropriate specialists.
Why Early Detection Matters for Your Neurological Health
Understanding your genetic status provides numerous benefits for your long-term wellbeing:
- Peace of Mind: Eliminate uncertainty about your genetic risk factors
- Proactive Planning: Work with neurologists to monitor and manage potential symptoms
- Family Insights: Understand inheritance patterns for family planning decisions
- Early Intervention: Access appropriate therapies and support services sooner
- Personalised Care: Receive tailored medical recommendations based on your genetic profile
Understanding Your Test Results with Compassion
We know that waiting for genetic test results can be anxiety-provoking. Our team provides clear, compassionate explanations of your results, whether they indicate a genetic mutation or provide reassuring information. Your results will include:
- Detailed analysis of SBF2 gene variations
- Interpretation of clinical significance
- Recommendations for next steps and specialist consultations
- Genetic counselling follow-up to discuss implications
- Resources for support and management if needed
Remember, genetic information is powerful knowledge that empowers you to take control of your health journey.
Transparent Pricing for Peace of Mind
| Service | Regular Price | Special Price |
|---|---|---|
| SBF2 Gene CMT4B2 NGS Genetic DNA Test | ZAR 6,700 | |
| Includes genetic counselling session and comprehensive result interpretation | ||
Considering the potential long-term healthcare costs of undiagnosed neurological conditions, this investment in your health provides exceptional value and peace of mind.
Why Trust Oracle Genomics with Your Genetic Testing?
We’ve built our reputation on accuracy, compassion, and accessibility:
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Advanced Technology: State-of-the-art NGS technology for unparalleled accuracy
- Expert Team: Collaboration with neurologists and genetic specialists
- Comprehensive Support: Genetic counselling included with every test
- Proven Track Record: Trusted by healthcare professionals nationwide
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about your neurological health create unnecessary anxiety. With results available in just 3-4 weeks and professional support throughout your journey, now is the time to gain the clarity you deserve.
Limited Time Special: Book now to secure your test at the special price of ZAR 6,700 – saving you ZAR 2,650 off the regular price. This offer includes your comprehensive genetic counselling session and detailed family pedigree analysis.
Early detection of hereditary neurological conditions can significantly improve quality of life and treatment outcomes. Don’t delay – take control of your genetic health journey today.
