Find Clarity for Unexplained Neurological Symptoms
When you’re experiencing mysterious neurological episodes, muscle weakness, or developmental delays, the uncertainty can be overwhelming. Our MELAS mutation detection test provides the answers you deserve, helping you understand whether mitochondrial disorders are affecting your health. For South Africans seeking neurological clarity, this test represents a crucial step toward proper diagnosis and management.
Understanding Your MELAS Genetic Test
MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes) is a complex genetic condition that affects how your body’s cells produce energy. Think of mitochondria as your body’s power plants – when they don’t function properly, it can lead to neurological symptoms that mimic strokes, muscle weakness, and other concerning health issues.
Our test specifically looks for genetic mutations that cause MELAS syndrome, using advanced PCR and sequencing technology that provides 99.9% accuracy. This isn’t just a test – it’s a pathway to understanding what’s happening inside your body at the cellular level.
Who Should Consider This Test?
This test could be life-changing if you or your loved one experiences:
- Unexplained stroke-like episodes without typical risk factors
- Progressive muscle weakness and fatigue
- Recurrent headaches or migraines
- Developmental delays in children
- Seizures or epilepsy of unknown origin
- Family history of mitochondrial disorders
- Unexplained lactic acidosis
- Vision or hearing problems with neurological symptoms
Many South African patients spend years searching for answers to these symptoms. Our test can provide the clarity needed to move forward with appropriate treatment and management strategies.
Why Early Detection Matters for Your Health
Getting a definitive diagnosis through genetic testing can transform your healthcare journey:
- End Diagnostic Uncertainty: Stop the cycle of unexplained symptoms and multiple specialist visits
- Personalised Treatment: Work with your neurologist to develop targeted management strategies
- Family Planning Insights: Understand inheritance patterns for future family planning decisions
- Prevent Complications: Early intervention can help manage symptoms and prevent disease progression
- Peace of Mind: Replace anxiety with understanding and a clear path forward
Understanding Your Results – We’re Here to Help
Receiving genetic test results can feel overwhelming, but you won’t be alone in this process. Your results will clearly indicate whether MELAS-associated mutations were detected, and our team provides:
- Easy-to-understand report formatting
- Direct consultation with your referring physician
- Guidance on next steps regardless of the outcome
- Support resources for positive results
- Reassurance and clarity for negative results
Remember: A positive result means you can finally take targeted action, while a negative result provides valuable information to explore other diagnostic possibilities.
Transparent Pricing – Investing in Your Health
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| MELAS Mutation Detection Test | ZAR 2,500 | ZAR 1,200 |
Consider this: The cost of ongoing specialist visits, unnecessary treatments, and lost productivity from undiagnosed symptoms often far exceeds this one-time investment in definitive answers.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Developed in consultation with leading South African neurologists
- Rapid Turnaround: Sample Monday by 9 AM, results by Friday
- Accuracy Guarantee: 99.9% detection rate using gold-standard PCR and sequencing methods
- Patient-Focused: Empathetic support throughout your testing journey
Take the First Step Toward Neurological Clarity
Don’t let uncertainty about your neurological health continue to impact your quality of life. With our special pricing of ZAR 2,500 (saving you ZAR 1,200), there’s never been a better time to get the answers you deserve.
Limited Time Offer: This special pricing of ZAR 2,500 won’t last forever. Take action today to secure your neurological health assessment at this exceptional value.
“Many patients tell us they wish they had taken this step sooner. The relief of having answers, whether positive or negative, is transformative for their healthcare journey.” – Oracle Genomics Patient Care Team
Test Specifications:
- Sample Required: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube
- Shipping: Refrigerated – DO NOT FREEZE
- Mandatory: Duly filled Genomics Clinical Information Requisition Form (Form 20)
- Turnaround: Sample Monday by 9 AM; Report Friday
- Methodology: PCR and Sequencing
- Specialty: Neurological Genetics
