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MT-TE Gene Mitochondrial Myopathy Infantile Transient Genetic DNA Test

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

-28%

The MT-TE Gene Mitochondrial Myopathy Infantile Transient Genetic DNA Test provides crucial early detection for infants at risk of mitochondrial disorders. For only ZAR 6,700 (regularly ZAR 9,350), this advanced NGS technology test offers peace of mind and accurate diagnosis for families across South Africa. Our comprehensive testing identifies mutations in the MT-TE gene that can cause temporary but serious muscle weakness and developmental concerns in infants. With results available in 3-4 weeks, you can take proactive steps to manage your child’s health. Oracle Genomics provides trusted genetic testing with nationwide coverage, ensuring accessibility for families in Johannesburg, Cape Town, Durban, and Pretoria. Our expert team includes cardiologists and genetic counsellors who provide compassionate support throughout the testing process. Early detection means better management and improved outcomes for your child’s health journey.

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

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
Guaranteed Safe Checkout

MT-TE Gene Mitochondrial Myopathy Test | ZAR 6
MT-TE Gene Mitochondrial Myopathy Infantile Transient Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Protecting Your Child’s Future: MT-TE Gene Mitochondrial Myopathy Testing

As a parent, nothing matters more than your child’s health and wellbeing. When your infant shows signs of muscle weakness or developmental concerns, the uncertainty can be overwhelming. Our MT-TE Gene Mitochondrial Myopathy Infantile Transient Genetic DNA Test provides the answers you need with the compassion you deserve.

For families across South Africa – from Johannesburg to Cape Town, Durban to Pretoria – we offer advanced genetic testing that brings clarity to complex health concerns. At only ZAR 6,700, this comprehensive test represents a vital investment in your child’s health journey.

Understanding the MT-TE Gene Test

Mitochondrial myopathy is a condition that affects the energy-producing parts of your cells, often causing muscle weakness and fatigue. The MT-TE gene plays a crucial role in this process, and when mutations occur, they can lead to temporary but significant health challenges in infants.

Our Next-Generation Sequencing (NGS) technology examines the MT-TE gene with exceptional accuracy, identifying specific mutations that might be causing your child’s symptoms. This isn’t just a test – it’s a pathway to understanding and managing your child’s health condition.

Who Should Consider This Test?

This test is particularly important for infants showing:

  • Unexplained muscle weakness or poor muscle tone
  • Feeding difficulties or poor weight gain
  • Developmental delays in motor skills
  • Family history of mitochondrial disorders
  • Temporary episodes of muscle function loss
  • Unexplained fatigue or lethargy

If your child has been experiencing these symptoms, early genetic testing can provide the clarity needed for appropriate medical management and intervention.

Why Early Detection Matters for Your Child’s Health

Identifying MT-TE gene mutations early provides numerous benefits:

  • Peace of Mind: Replace uncertainty with clear understanding of your child’s condition
  • Targeted Treatment: Enable healthcare providers to develop appropriate management plans
  • Family Planning: Understand genetic risks for future pregnancies
  • Proactive Care: Implement early interventions that can improve outcomes
  • Reduced Anxiety: Knowledge replaces fear with actionable information

Understanding Your Test Results

We understand that waiting for genetic test results can be stressful. Our team provides:

  • Clear Explanations: Simple, understandable reports that explain what the results mean
  • Genetic Counselling: Professional guidance to help you understand the implications
  • Family Pedigree Analysis: Mapping your family history to provide context
  • Next Steps Guidance: Clear recommendations for managing your child’s health
  • Ongoing Support: Access to our team for any follow-up questions

Your results will be available within 3-4 weeks, and we’ll guide you through every step of understanding them.

Affordable, Accessible Genetic Testing

Test Feature Details Value
Regular Price ZAR 9,350 Comprehensive genetic analysis
Special Price ZAR 6,700 Limited time savings of ZAR 2,650
Turnaround Time 3-4 Weeks Timely results for prompt action
Sample Type Blood, Extracted DNA, or Blood on FTA Card Convenient testing options
Technology NGS (Next-Generation Sequencing) Gold standard accuracy

Consider this: early detection can prevent years of uncertainty and potentially reduce long-term healthcare costs. This test represents exceptional value for your child’s health future.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Our tests are developed and interpreted by specialist cardiologists
  • Advanced Technology: NGS technology ensures 99.9% accuracy in genetic analysis
  • Genetic Counselling: Comprehensive support before, during, and after testing
  • Patient-Focused Care: We understand the emotional journey of genetic testing
  • Proven Track Record: Trusted by healthcare providers across South Africa

Take the First Step Toward Clarity

Don’t let uncertainty about your child’s health create unnecessary stress. Early detection through genetic testing provides the information needed to make informed decisions about their care.

Book your MT-TE Gene Mitochondrial Myopathy Test today for only ZAR 6,700 and give your child the gift of clarity and proactive healthcare.

Our team is ready to support you through this important health journey. Contact us now to schedule your test or speak with our genetic counselling team.



Limited time special pricing available. Don’t delay your child’s health assessment.