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GJB1 Gene Dejerine-Sottas Disease NGS Genetic DNA Test

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

-28%

If you’re experiencing unexplained muscle weakness, numbness, or coordination difficulties, our GJB1 Gene Dejerine-Sottas Disease NGS Genetic DNA Test provides the answers you need. This comprehensive test uses advanced Next-Generation Sequencing technology to detect mutations in the GJB1 gene, which is responsible for this rare inherited neurological condition. For just ZAR 6,700 (regularly ZAR 9,350), you’ll receive accurate, reliable results within 4-5 weeks. Our test helps identify the genetic cause of your symptoms, enabling better management strategies and providing peace of mind for you and your family. With genetic counselling included and nationwide coverage across South Africa, we make this important health investigation accessible and stress-free.

📞 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

GJB1 Gene Dejerine-Sottas Disease DNA Test | ZAR 6
GJB1 Gene Dejerine-Sottas Disease NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Answers for Unexplained Neurological Symptoms

Living with unexplained muscle weakness, numbness, or coordination problems can be frightening and isolating. You may have visited multiple doctors, tried various treatments, but still lack clear answers about what’s causing your symptoms. Our GJB1 Gene Dejerine-Sottas Disease NGS Genetic DNA Test provides the clarity you deserve, using cutting-edge technology to identify the genetic root of your neurological concerns.

Understanding Your GJB1 Gene Test

Dejerine-Sottas disease is a rare inherited neurological condition that affects the peripheral nerves, causing progressive muscle weakness and sensory loss. The GJB1 gene provides instructions for making a protein essential for proper nerve function. When mutations occur in this gene, it disrupts nerve signal transmission, leading to the symptoms of Dejerine-Sottas disease.

Our test uses Next-Generation Sequencing (NGS) technology, the gold standard in genetic testing, to thoroughly examine your GJB1 gene for any abnormalities. This advanced approach ensures maximum accuracy and reliability in detecting even subtle genetic variations.

Who Should Consider This Test?

This test is particularly important if you experience:

  • Progressive muscle weakness in hands, feet, or limbs
  • Numbness or tingling sensations
  • Difficulty with coordination and balance
  • Foot deformities or high arches
  • Family history of similar neurological symptoms
  • Unexplained walking difficulties
  • Muscle atrophy or wasting

If these symptoms sound familiar, or if you have family members with similar concerns, this test could provide the answers that have been eluding you.

Why Early Detection Matters for Your Health

Getting a definitive diagnosis through genetic testing offers several crucial benefits:

  • Personalised Management: Knowing the specific genetic cause allows for tailored treatment and management strategies
  • Family Planning: Understand inheritance patterns and make informed decisions about family planning
  • Peace of Mind: End the uncertainty and anxiety of not knowing what’s causing your symptoms
  • Proactive Care: Early detection enables proactive monitoring and intervention to manage symptoms effectively
  • Genetic Counselling: Our included genetic counselling helps you understand results and implications for your family

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. Our team ensures you receive clear, comprehensive results with professional guidance:

  • Clear Reporting: Results presented in easy-to-understand language with medical interpretation
  • Professional Support: Genetic counsellors available to explain findings and answer questions
  • Actionable Insights: Practical recommendations based on your specific results
  • Family Implications: Guidance on what results mean for your relatives
  • Next Steps: Clear direction for follow-up care and management

Remember, a positive result doesn’t define your future – it empowers you to take control of your health journey.

Transparent Pricing & Exceptional Value

Service Regular Price Special Price Savings
GJB1 Gene Dejerine-Sottas Disease NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Genetic Counselling Session Included at no extra cost
Family Pedigree Analysis Included at no extra cost

Turnaround Time: 4-5 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card

Why Trust Oracle Genomics?

We’ve built our reputation on accuracy, compassion, and accessibility:

  • Nationwide Coverage: Serving patients across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: Using NGS technology for maximum accuracy and reliability
  • Patient-Centred Care: We prioritise your comfort, understanding, and peace of mind
  • Comprehensive Support: From initial consultation through to results explanation and beyond

Take the First Step Toward Clarity Today

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

What’s Included:

  • Comprehensive GJB1 gene analysis using NGS technology
  • Professional genetic counselling session
  • Family pedigree chart analysis
  • Clear, comprehensive results explanation
  • Nationwide accessibility across South Africa

Ready to Begin? Contact us today to schedule your test and take control of your neurological health. Our caring team is ready to support you every step of the way.



Limited time special pricing available. Don’t delay your journey to answers and peace of mind.