Find Answers for Unexplained Muscle Weakness
When every movement feels like a struggle and muscle weakness impacts your daily life, getting clear answers becomes essential. Our comprehensive genetic test for Bethlem Myopathy, Myofibrillar Myopathy, and Ullrich Muscular Dystrophy provides the definitive diagnosis you’ve been searching for, giving you the power to take control of your health journey.
Understanding Your Genetic Test
This advanced Next-Generation Sequencing test examines 9 critical genes responsible for these rare muscular conditions. By analysing your DNA, we can identify specific genetic mutations that cause progressive muscle weakness, joint contractures, and mobility challenges. The test provides 99.9% accuracy using both NGS and Sanger sequencing methods, ensuring you receive reliable, trustworthy results.
Who Should Consider This Test?
If you experience any of these symptoms, this test could provide life-changing answers:
- Progressive muscle weakness starting in childhood or adulthood
- Joint stiffness or contractures that limit movement
- Difficulty with walking, climbing stairs, or rising from chairs
- Family history of muscular disorders
- Unexplained fatigue during physical activity
- Delayed motor milestones in children
Many South Africans in Johannesburg, Cape Town, and Durban have found clarity through this testing, enabling proper treatment and management strategies.
Why Early Detection Matters for Your Health
Getting an accurate diagnosis transforms your healthcare journey. Early detection allows for:
- Proper Treatment Planning: Tailored physical therapy and medical interventions
- Family Risk Assessment: Understanding inheritance patterns for family planning
- Peace of Mind: Ending the uncertainty and anxiety of not knowing
- Improved Quality of Life: Better management of symptoms and progression
- Access to Support: Connecting with appropriate medical specialists and support groups
Understanding Your Results with Compassion
We know waiting for genetic results can be anxiety-provoking. Our team provides clear, compassionate explanations of your findings. You’ll receive:
- Comprehensive report explaining your genetic variants
- Guidance on what your results mean for your health
- Recommendations for next steps and specialist referrals
- Support in understanding inheritance patterns
- Access to genetic counselling if needed
Results are typically available within 40 working days, and our team is here to support you throughout the process.
Transparent Pricing – Your Health Investment
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| Comprehensive Genetic Analysis | ZAR 8,700 | ZAR 7,800 | ZAR 900 |
This investment in your health provides lifelong clarity and enables proper medical management that could save thousands in future healthcare costs.
Why Trust Oracle Genomics?
- Nationwide Coverage: Serving patients across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: Using cutting-edge NGS and Sanger sequencing for maximum accuracy
- Patient-Focused Care: Compassionate support throughout your testing journey
- Proven Accuracy: 99.9% reliability in genetic variant detection
Take the First Step Toward Clarity Today
Don’t let uncertainty about your muscle health continue to impact your life. With convenient testing locations nationwide and compassionate support every step of the way, getting answers has never been easier.
Sample Requirements: 10 mL whole blood from 2 Lavender Top (EDTA) tubes. Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory. Samples accepted daily by 9 am.
Limited Time Special: Save ZAR 900 on your comprehensive genetic analysis. Early detection leads to better outcomes – don’t delay getting the answers you deserve.
