Find Clarity for Unexplained Movement Difficulties
When simple tasks like walking, balancing, or coordinating movements become challenging without clear explanation, it can be frightening and isolating. The RUBCN Gene Salih Ataxia NGS Genetic DNA Test offers the answers you deserve, using cutting-edge technology to identify hereditary factors that may be affecting your neurological health.
Understanding Your RUBCN Gene Test
This specialised genetic test examines the RUBCN gene using Next-Generation Sequencing (NGS) technology, the most advanced method available for detecting genetic mutations. The RUBCN gene plays a crucial role in neurological function, and specific mutations can lead to Salih ataxia – a hereditary condition affecting coordination and movement.
Our test doesn’t just provide results; it offers understanding. Through comprehensive genetic counselling, we help map your family’s health history, creating a clear picture that puts your results in meaningful context.
Who Should Consider This Test?
This test is particularly important if you experience:
- Unexplained balance problems or frequent stumbling
- Difficulty with coordination in daily activities
- Progressive walking difficulties without clear cause
- Family history of movement disorders or ataxia
- Neurological symptoms that multiple doctors haven’t been able to diagnose
If you’ve been searching for answers about persistent movement challenges, this test could provide the clarity that transforms your healthcare journey.
Why Early Detection Matters for Your Health
Identifying RUBCN gene mutations early provides significant advantages:
- Peace of Mind: End the uncertainty about your symptoms and receive a clear diagnosis
- Proactive Management: Develop targeted strategies to manage symptoms and maintain quality of life
- Family Planning Insights: Understand hereditary risks for future generations
- Treatment Guidance: Work with neurologists to create personalised care plans
- Emotional Relief: Replace fear and confusion with knowledge and control
Understanding Your Test Results
We know waiting for genetic test results can be anxiety-provoking. That’s why we provide:
- Clear Explanations: Results presented in easy-to-understand language
- Expert Interpretation: Professional analysis from our genetic specialists
- Actionable Guidance: Specific recommendations based on your results
- Ongoing Support: Access to resources and follow-up consultations
Whether your results indicate a genetic mutation or provide reassuring clarity, you’ll receive the support and guidance needed to move forward confidently.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| RUBCN Gene Salih Ataxia NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Includes genetic counselling session and comprehensive result interpretation | |||
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why Trust Oracle Genomics?
We understand that genetic testing involves more than just science – it involves trust, empathy, and professional excellence.
- Nationwide Coverage: Accessible testing centres across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialist neurologists and genetic counsellors overseeing every test
- Advanced Technology: State-of-the-art NGS technology ensuring 99.9% accuracy
- Patient-Centred Care: Empathetic support throughout your testing journey
- Proven Track Record: Thousands of South Africans trust us with their genetic health
Take Control of Your Neurological Health Today
Don’t let uncertainty about movement difficulties control your life. The answers you need are within reach, and taking action now could make all the difference in your health journey.
Limited Time Offer: Secure your special pricing of ZAR 6,700 before this offer ends. Your journey to clarity and peace of mind starts with one simple decision.
