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MT-TS1 Gene MERRF/MELAS Overlap Syndrome Genetic DNA Test

Original price was: R9,350.Current price is: R6,700.

-28%

If you’re experiencing unexplained neurological symptoms or have a family history of mitochondrial disorders, the MT-TS1 Gene MERRF/MELAS Overlap Syndrome Genetic DNA Test provides the clarity you need. This comprehensive test uses advanced NGS technology to detect mutations in the MT-TS1 gene, which can cause complex neurological conditions affecting muscle function, brain development, and overall energy production. For just ZAR 6,700 (regularly ZAR 9,350), you’ll receive accurate, reliable results within 3-4 weeks. Our test helps identify the root cause of symptoms like muscle weakness, seizures, developmental delays, and fatigue, giving you and your healthcare team the information needed for proper management and treatment planning. With nationwide coverage across South Africa including Johannesburg, Cape Town, Durban, and Pretoria, accessing this specialised genetic testing has never been easier. Take control of your neurological health today with confidence in our medical expertise and commitment to patient care.

📞 24/7 South African Support Team Call : +27 6412 56421

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
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MT-TS1 Genetic Test ZAR 6
MT-TS1 Gene MERRF/MELAS Overlap Syndrome Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Answers for Complex Neurological Symptoms

When you’re facing unexplained muscle weakness, seizures, or developmental concerns, it can feel overwhelming and isolating. The MT-TS1 Gene MERRF/MELAS Overlap Syndrome Genetic DNA Test provides the clarity and answers you’ve been searching for, helping you understand the genetic factors behind your neurological health challenges.

Understanding Your MT-TS1 Genetic Test

This specialised test examines the MT-TS1 gene using Next-Generation Sequencing (NGS) technology, the most advanced method available for genetic analysis. The MT-TS1 gene plays a crucial role in mitochondrial function – the energy powerhouses of your cells. When mutations occur in this gene, they can lead to overlapping symptoms of MERRF (Myoclonic Epilepsy with Ragged-Red Fibers) and MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes) syndromes.

Our test doesn’t just provide results – it gives you and your neurologist a clear roadmap for understanding your condition and developing an effective management plan.

Who Should Consider This Genetic Test?

This test is particularly important if you or your loved one experiences:

  • Unexplained muscle weakness or fatigue that worsens with activity
  • Recurrent seizures or myoclonus (muscle jerks)
  • Developmental delays in children or cognitive changes in adults
  • Stroke-like episodes without typical risk factors
  • Family history of mitochondrial disorders or similar neurological conditions
  • Unexplained hearing loss or vision problems
  • Exercise intolerance that seems disproportionate to your fitness level

Many patients find relief in finally having a name for their symptoms and a clear path forward.

Why Early Detection Matters for Your Health

Getting an accurate diagnosis through genetic testing can transform your healthcare journey:

  • Personalised Treatment: Your neurologist can develop targeted treatment strategies based on your specific genetic profile
  • Family Planning: Understand inheritance patterns and make informed decisions about family planning
  • Symptom Management: Better manage symptoms with appropriate medications and lifestyle adjustments
  • Peace of Mind: Reduce the stress of uncertainty and multiple doctor visits searching for answers
  • Prevent Complications: Early intervention can help prevent or minimise serious complications

Understanding Your Test Results

We know waiting for genetic test results can be anxiety-provoking. That’s why we provide clear, comprehensive reports that your neurologist can easily interpret and explain to you. Your results will clearly indicate:

  • Whether MT-TS1 gene mutations were detected
  • The specific type of mutation found (if any)
  • What the results mean for your health and treatment options
  • Recommendations for next steps in your care

Our genetic counselling support ensures you fully understand your results and their implications for you and your family.

Transparent Pricing – Exceptional Value

Test Option Price Savings
Special Offer Price ZAR 6,700 ZAR 2,650 OFF
Regular Price ZAR 9,350

What’s Included:

  • Comprehensive MT-TS1 gene analysis using NGS technology
  • Detailed results report with clinical interpretation
  • Genetic counselling session to discuss results
  • Sample collection (blood or DNA sample)
  • 3-4 week turnaround time
  • Ongoing support from our medical team

Considering the cost of ongoing specialist visits and unnecessary treatments, this test represents significant long-term healthcare savings.

Why Trust Oracle Genomics?

Nationwide Accessibility: We serve patients across South Africa with convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria, and surrounding areas.

Medical Expertise: Our tests are developed and interpreted by specialist neurologists and genetic experts with years of experience in mitochondrial disorders.

Accuracy Guarantee: We use only the most advanced NGS technology, ensuring the highest accuracy rates in genetic testing.

Patient-Centred Care: From sample collection to results explanation, we prioritise your comfort, understanding, and emotional wellbeing.

Complete Preparation Support: We guide you through the clinical history documentation and pedigree chart creation to ensure comprehensive testing.

Take the First Step Toward Clarity Today

Don’t let uncertainty about your neurological health continue to impact your quality of life. With our special pricing of ZAR 6,700, there’s never been a better time to get the answers you deserve.

Limited Time Offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) is available for a limited time. Don’t delay getting the clarity that could transform your healthcare journey.

“Finally understanding my genetic condition changed everything. The team at Oracle Genomics made the process clear and supportive every step of the way.” – Recent Patient