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Next Generation Sequencing Alexander Disease Test

Original price was: R8,700.Current price is: R7,800.

-10%

Facing neurological symptoms or family history concerns? Our Next Generation Sequencing Alexander Disease Test provides definitive answers with 99.9% accuracy. For just ZAR 7,800 (regularly ZAR 8,700), this comprehensive genetic analysis detects GFAP gene mutations that cause Alexander Disease – a rare neurological disorder affecting brain development. Our advanced NGS technology ensures precise results within 40 working days, giving you the clarity needed for proper medical management. Available across South Africa including Johannesburg, Cape Town, and Durban, this test brings peace of mind through early detection and expert interpretation by qualified neurologists. Take control of your neurological health today with trusted genetic testing from Oracle Genomics.

📞 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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Alexander Disease Genetic Test ZAR 7
Next Generation Sequencing Alexander Disease Test
R8,700 Original price was: R8,700.R7,800Current price is: R7,800.

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Find Clarity for Neurological Concerns with Alexander Disease Genetic Testing

When you or your loved one experiences unexplained neurological symptoms, the uncertainty can be overwhelming. Our Next Generation Sequencing Alexander Disease Test provides the definitive answers you need to move forward with confidence. For South African families seeking clarity about rare neurological conditions, this advanced genetic analysis offers peace of mind through precise, reliable results.

Understanding Alexander Disease Genetic Testing

Alexander Disease is a rare genetic disorder that affects the nervous system, primarily impacting brain development and function. Our test uses cutting-edge Next Generation Sequencing (NGS) technology to analyze the GFAP gene – the specific gene responsible for this condition. Unlike basic genetic screens, our comprehensive approach examines the entire gene sequence, ensuring no mutation goes undetected.

The process is straightforward: we analyze a small blood sample using both NGS and Sanger sequencing methods for confirmation. This dual-approach guarantees 99.9% accuracy, giving you and your healthcare provider the reliable information needed for proper diagnosis and management.

Who Should Consider This Important Genetic Test?

This test is specifically designed for individuals and families experiencing:

  • Unexplained developmental delays in infants and children
  • Progressive neurological symptoms including seizures or motor difficulties
  • Family history of Alexander Disease or similar neurological conditions
  • Abnormal brain imaging results suggesting white matter disorders
  • Concerns about genetic inheritance patterns for family planning

If you’ve been searching for answers about mysterious neurological symptoms, this test could provide the breakthrough understanding you need.

Why Early Detection Matters for Your Health Journey

Getting a definitive diagnosis through genetic testing transforms uncertainty into actionable knowledge. The benefits extend far beyond simple confirmation:

  • Personalized Treatment Planning: Accurate diagnosis enables targeted medical management and appropriate interventions
  • Family Planning Guidance: Understand inheritance patterns to make informed decisions about future pregnancies
  • Reduced Diagnostic Odyssey: Avoid years of uncertainty and multiple specialist visits
  • Emotional Peace of Mind: Replace anxiety with clarity and a clear path forward
  • Access to Specialized Care: Connect with neurologists and genetic counselors who understand your specific condition

Understanding Your Test Results with Confidence

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive support throughout the process:

Clear, Understandable Reports: Your results will be presented in easy-to-understand language, with clear explanations of any findings.

Expert Interpretation: Our qualified neurologists and genetic specialists review every result to ensure accurate interpretation.

Genetic Counseling Support: We can connect you with genetic counseling services to help you understand the implications of your results.

Medical Follow-up Guidance: Receive clear recommendations for next steps based on your specific results.

Remember: A positive result provides the information needed for proper management, while a negative result brings valuable peace of mind.

Transparent Pricing – Exceptional Value for Your Health

Test Description Regular Price Special Price Savings
Next Generation Sequencing Alexander Disease Test ZAR 8,700 ZAR 7,800 ZAR 900

Turnaround Time: Sample collection daily by 9 AM | Results in 40 working days

Sample Requirements: 10 mL (5 mL minimum) whole blood from 2 Lavender Top (EDTA) tubes. Ship refrigerated. DO NOT FREEZE.

Mandatory Preparation: Duly filled Whole Exome Sequencing Consent Form (Form 37) is required.

Why Thousands of South Africans Trust Oracle Genomics

Nationwide Coverage

Convenient testing available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria

Medical Expertise

Tests reviewed and interpreted by qualified neurologists and pediatric specialists

Advanced Technology

State-of-the-art NGS and Sanger sequencing for 99.9% accuracy

Patient-Centred Care

Empathetic support throughout your testing journey

Take the First Step Toward Clarity Today

Don’t let uncertainty about neurological symptoms control your life. Our Alexander Disease genetic test provides the answers you need to make informed healthcare decisions.

Limited Time Offer: Save ZAR 900 on this comprehensive genetic analysis. Early detection can make all the difference in managing neurological conditions effectively.

“Finally getting answers after years of uncertainty gave our family the direction we needed.” – Satisfied Oracle Genomics Patient