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RAB7A Gene CMT2B NGS Genetic DNA Test

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

-28%

If you’re experiencing unexplained muscle weakness, foot deformities, or have a family history of Charcot-Marie-Tooth disease, our RAB7A Gene CMT2B NGS Genetic DNA Test provides the answers you need for just ZAR 6,700. This comprehensive test uses advanced Next Generation Sequencing technology to detect mutations in the RAB7A gene, which is responsible for CMT2B – a hereditary form of peripheral neuropathy. Early detection can help you understand your risk, make informed health decisions, and potentially slow disease progression. Our test includes professional genetic counselling to help you understand your family history and results. With nationwide coverage across South Africa including Johannesburg, Cape Town, and Durban, you can trust Oracle Genomics for accurate, reliable genetic testing that puts your health first.

📞 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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RAB7A Gene CMT2B DNA Test | ZAR 6
RAB7A Gene CMT2B NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity About Hereditary Neuropathy with Our RAB7A Gene CMT2B DNA Test

Living with unexplained muscle weakness, numbness, or foot problems can be frightening, especially when it runs in your family. If you’ve been searching for answers about Charcot-Marie-Tooth disease or suspect you might be at risk, our RAB7A Gene CMT2B NGS Genetic DNA Test provides the clarity and peace of mind you deserve. For just ZAR 6,700, you can take control of your health journey with South Africa’s most trusted genetic testing service.

Understanding Your RAB7A Gene CMT2B Test

The RAB7A gene plays a crucial role in your nervous system’s health, specifically in the peripheral nerves that control movement and sensation in your arms and legs. When mutations occur in this gene, it can lead to Charcot-Marie-Tooth disease type 2B (CMT2B), a hereditary condition that affects nerve function. Our test uses advanced Next Generation Sequencing (NGS) technology to examine your RAB7A gene with exceptional accuracy, giving you reliable results you can trust for making important health decisions.

Who Should Consider This Test?

This test is particularly important if you experience:

  • Unexplained muscle weakness in your feet, legs, or hands
  • Foot deformities like high arches or hammertoes
  • Numbness, tingling, or reduced sensation in your extremities
  • Difficulty with balance or frequent tripping
  • A family history of Charcot-Marie-Tooth disease or similar neurological conditions
  • Progressive loss of muscle tissue in your lower legs or hands

If any of these symptoms sound familiar, or if CMT2B runs in your family, this test could provide the answers you need to manage your health proactively.

Why Early Detection Matters for Your Health

Getting tested for RAB7A gene mutations offers significant benefits for your long-term wellbeing:

  • Peace of Mind: Eliminate uncertainty about your genetic risk and family planning decisions
  • Early Intervention: Begin appropriate management strategies before symptoms progress
  • Family Planning: Make informed decisions about having children and their potential risk
  • Personalised Care: Work with your neurologist to create a tailored treatment plan
  • Prevent Complications: Address foot problems and mobility issues before they become severe

Knowledge is power when it comes to hereditary conditions, and early detection can significantly improve your quality of life.

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. That’s why we provide clear, comprehensive reports with expert guidance. Your results will clearly indicate whether RAB7A gene mutations were detected, and our genetic counselling team will help you understand what this means for your health. Whether your results are positive or negative, you’ll receive personalised recommendations for next steps and ongoing care.

Turnaround Time: 3 to 4 weeks from sample receipt

Sample Options: Blood sample, extracted DNA, or one drop of blood on FTA card

Affordable, Accessible Genetic Testing

Test Option Price Value
Regular Price ZAR 9,350 Comprehensive genetic analysis
Special Price ZAR 6,700 Save ZAR 2,650

Your investment includes not just the advanced NGS testing, but also professional genetic counselling to help create your family pedigree chart and interpret your results in the context of your family history.

Why Trust Oracle Genomics?

As South Africa’s leading genetic testing provider, we’re committed to your health and peace of mind:

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Expert Collaboration: Working with qualified neurologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS testing for maximum accuracy
  • Patient-Centred Care: Empathetic support throughout your testing journey
  • Proven Reliability: Trusted by healthcare professionals nationwide

Take the First Step Toward Clarity Today

Don’t let uncertainty about hereditary neuropathy control your life. With our RAB7A Gene CMT2B test, you can get the answers you need to make informed decisions about your health and future.

Book your test now while the special price of ZAR 6,700 is available. Our team is ready to guide you through the process and provide the compassionate care you deserve.

Contact Oracle Genomics today to schedule your genetic counselling session and testing. Your journey to understanding begins here.