Understanding Your Risk for Neurofibromatosis Type 2
Living with uncertainty about genetic conditions can be overwhelming, especially when it involves conditions like neurofibromatosis type 2 that may affect your hearing, balance, and overall quality of life. We understand the anxiety that comes with potential genetic risks, and we’re here to provide the clarity and support you need through our comprehensive NF2 genetic testing service.
What This Test Detects
The NF2 Gene Neurofibromatosis Type 2 NGS Genetic DNA Test uses advanced Next-Generation Sequencing (NGS) technology to examine the NF2 gene for mutations that cause neurofibromatosis type 2. This condition typically leads to the development of benign tumours on the nerves that control hearing and balance, often resulting in hearing loss, tinnitus, and balance problems.
Our test provides precise genetic information that helps identify whether you carry the NF2 gene mutation, giving you and your healthcare provider valuable insights for proactive health management.
Who Should Consider This Test?
This test is particularly important if you experience:
- Gradual hearing loss, especially in one ear
- Tinnitus (ringing in the ears)
- Balance difficulties or dizziness
- Facial weakness or numbness
- Vision changes or cataracts at a young age
- Family history of neurofibromatosis type 2
- Personal history of benign nerve tumours
Even if you’re not experiencing symptoms but have a family member with NF2, genetic testing can provide crucial information about your own risk and help with family planning decisions.
Why Early Detection Matters for Your Health
Knowing your genetic status empowers you to take control of your health journey. Early detection of NF2 gene mutations allows for:
- Proactive monitoring and early intervention
- Better management of symptoms as they develop
- Informed decisions about treatment options
- Reduced anxiety through certainty and knowledge
- Family planning with complete information
- Access to appropriate specialist care when needed
Peace of mind comes from understanding your genetic makeup and having a clear path forward for your healthcare.
Understanding Your Test Results
We know waiting for genetic test results can be stressful. Our team provides comprehensive support throughout the process:
- Clear Results: You’ll receive easy-to-understand results explaining whether an NF2 gene mutation was detected
- Professional Guidance: Our genetic counsellors help interpret your results and discuss next steps
- Medical Referral: If needed, we’ll connect you with appropriate specialists for ongoing care
- Family Implications: We’ll explain what your results mean for your family members
Remember, a positive result doesn’t mean symptoms will definitely develop, but it does mean you can be proactive about your health monitoring.
Transparent Pricing & Value
| Service | Regular Price | Special Price |
|---|---|---|
| NF2 Genetic DNA Test | ZAR 9,350 | ZAR 6,700 |
| Includes genetic counselling | Included | |
| Turnaround time | 3-4 weeks | |
Consider the value: Early detection can help prevent costly complications and provide peace of mind that’s truly priceless. Many private medical aids may cover genetic testing when medically indicated.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Specialised oncologists and genetic counsellors overseeing your care
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Comprehensive Support: Genetic counselling included with every test
- Proven Track Record: Trusted by healthcare professionals nationwide
Take the First Step Toward Clarity
Don’t let uncertainty about genetic risks control your life. Our NF2 genetic test provides the answers you need to make informed decisions about your health future.
Book your test today and receive:
- Professional genetic counselling session
- Comprehensive family history assessment
- Clear, easy-to-understand results
- Ongoing support and guidance
Contact us now to schedule your appointment or speak with our genetic counselling team. Your journey to genetic clarity starts here.
Test Preparation & Sample Collection
We make the testing process as simple and comfortable as possible:
- Sample Options: Blood draw, extracted DNA, or simple finger-prick blood spot
- Preparation: Bring your clinical history and family medical information
- Genetic Counselling: Included session to create your family pedigree chart
- Convenience: Multiple sample collection methods to suit your preference
