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SLC25A4 Gene Progressive External Ophthalmoplegia Genetic DNA Test

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

-28%

If you’re experiencing progressive eye muscle weakness, drooping eyelids, or difficulty moving your eyes, our SLC25A4 gene test provides the answers you need. This comprehensive genetic DNA test specifically detects progressive external ophthalmoplegia with mitochondrial deletions type 2, an autosomal dominant condition that can significantly impact your quality of life. For just R6,700 (regularly R9,350), you’ll receive precise results within 3-4 weeks using advanced NGS technology. Our test is crucial for South African families with a history of mitochondrial disorders, helping you understand your genetic risk and make informed health decisions. With nationwide coverage including Johannesburg, Cape Town, and Durban, we make genetic testing accessible and trustworthy. Take control of your neurological health today with confidence in our medical expertise and commitment to accuracy.

📞 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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SLC25A4 Gene Test R6
SLC25A4 Gene Progressive External Ophthalmoplegia Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Eye Muscle Weakness: SLC25A4 Gene Testing for Progressive External Ophthalmoplegia

If you’ve noticed progressive weakness in your eye muscles, drooping eyelids, or difficulty moving your eyes, you’re not alone. These symptoms can be frightening and isolating, but understanding their genetic cause is the first step toward managing your condition effectively. Our SLC25A4 gene test provides the clarity you need to address progressive external ophthalmoplegia with mitochondrial deletions type 2, giving you back control over your neurological health.

What This Test Detects

The SLC25A4 gene test specifically identifies mutations associated with progressive external ophthalmoplegia type 2, an autosomal dominant mitochondrial disorder. This means the condition can be passed from one generation to the next, with each child having a 50% chance of inheriting the affected gene. Using advanced Next-Generation Sequencing (NGS) technology, we analyse your DNA with exceptional accuracy to detect even subtle genetic variations that could be affecting your eye muscle function and overall mitochondrial health.

Who Should Consider This Test?

This test is essential if you experience:

  • Progressive weakness of eye muscles affecting movement
  • Drooping eyelids (ptosis) that worsens over time
  • Difficulty with eye coordination and tracking
  • Family history of mitochondrial disorders
  • Unexplained muscle weakness beyond the eyes
  • Progressive difficulty with activities requiring eye movement

If multiple family members show similar symptoms across generations, genetic testing becomes increasingly important for accurate diagnosis and family planning.

Why Early Detection Matters for Your Health

Receiving a definitive diagnosis through genetic testing provides numerous benefits:

  • Peace of Mind: End the uncertainty about your symptoms and their cause
  • Accurate Treatment Planning: Work with your neurologist to develop targeted management strategies
  • Family Planning Guidance: Understand inheritance patterns for informed reproductive decisions
  • Proactive Health Management: Monitor and address potential complications early
  • Reduced Medical Costs: Avoid unnecessary tests and treatments through precise diagnosis

Understanding Your Test Results

We know waiting for genetic test results can be anxiety-provoking. Our team provides clear, compassionate explanations of your findings:

  • Positive Result: Indicates the presence of SLC25A4 gene mutation. Our genetic counsellors will explain what this means for your health and connect you with appropriate specialists
  • Negative Result: No mutation detected, providing reassurance about this specific condition
  • Uncertain Variant: Rare genetic changes of unknown significance will be thoroughly explained with recommendations for monitoring

Every result includes a comprehensive consultation to ensure you fully understand the implications and next steps.

Transparent Pricing & Value

Service Regular Price Special Price Savings
SLC25A4 Gene Test R9,350 R6,700 R2,650
Turnaround Time 3-4 Weeks
Sample Type Blood, Extracted DNA, or Blood on FTA Card

This investment in your health can save thousands in unnecessary medical expenses and provide priceless peace of mind.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Specialised neurological genetic testing interpreted by qualified professionals
  • Advanced Technology: State-of-the-art NGS methodology for maximum accuracy
  • Genetic Counselling: Comprehensive pre- and post-test counselling included
  • Proven Accuracy: Reliable results you can trust for life-changing decisions

Take Control of Your Neurological Health Today

Don’t let uncertainty about your eye muscle weakness control your life. Early detection through genetic testing provides the answers you need to move forward with confidence. Our special pricing of R6,700 makes this crucial testing accessible to South African families.

Book your test now and receive:

  • Comprehensive genetic counselling session
  • Family pedigree analysis
  • Clear, understandable results explanation
  • Connection to appropriate medical specialists
  • Peace of mind about your genetic health

Contact us today to schedule your SLC25A4 gene test and take the first step toward understanding your neurological health.