Find Clarity About Cerebral Cavernous Malformations with CCM2 Gene Testing
When you’re concerned about neurological conditions running in your family, the uncertainty can feel overwhelming. Our CCM2 Gene Test provides the definitive answers you need to understand your risk for cerebral cavernous malformations type 2. Using advanced Next-Generation Sequencing technology, we deliver accurate, reliable results that empower you to take control of your neurological health.
Understanding the CCM2 Gene Test
The CCM2 Gene Test is a sophisticated genetic analysis that examines your DNA for mutations in the CCM2 gene, which is responsible for cerebral cavernous malformations type 2. These are abnormal clusters of blood vessels in the brain that can cause serious neurological symptoms. Our test uses NGS (Next-Generation Sequencing) technology, the gold standard in genetic testing, to provide comprehensive analysis with exceptional accuracy.
What makes our approach different is the inclusion of genetic counselling before testing. Our specialists will work with you to create a detailed family pedigree chart, helping us understand your complete genetic background and ensuring the most accurate interpretation of your results.
Who Should Consider This Test?
This test is particularly important if you experience:
- Recurrent headaches or migraines
- Seizures or unexplained neurological symptoms
- Family history of cerebral cavernous malformations
- Unexplained strokes or bleeding in the brain
- Vision problems or coordination issues
- Planning for pregnancy with family history of neurological conditions
If you have relatives diagnosed with cerebral cavernous malformations, this test can provide crucial information about your own risk and help guide preventive healthcare decisions.
Why This Test Matters for Your Health
Early detection of CCM2 gene mutations can be life-changing. By understanding your genetic risk, you can:
- Work with your healthcare provider to develop a proactive monitoring plan
- Make informed decisions about family planning
- Reduce anxiety through definitive knowledge
- Access appropriate medical care before symptoms become severe
- Potentially prevent serious neurological complications
- Provide valuable information for other family members
Many patients find that knowing their genetic status brings tremendous peace of mind, even if the results indicate increased risk.
Understanding Your Results
We know waiting for genetic test results can be stressful, which is why we provide clear, compassionate explanations of your findings. Your results will clearly indicate whether a CCM2 gene mutation was detected, and our genetic counsellors are available to help you understand what this means for your health.
If a mutation is found, we’ll provide detailed information about what this means for your risk level and connect you with resources for ongoing care. If no mutation is detected, you’ll have the reassurance of knowing your risk is significantly lower.
Remember: A positive result doesn’t mean you’ll definitely develop symptoms, but it does provide valuable information for proactive healthcare management.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| CCM2 Gene Test with Genetic Counselling | ZAR 6,700 |
Your investment includes:
- Comprehensive genetic counselling session
- Family pedigree chart creation
- Advanced NGS genetic testing
- Detailed results report
- Post-test consultation if needed
- Results in 3-4 weeks
Considering the potential to prevent serious neurological events, this test represents excellent value for your long-term health.
Why Trust Oracle Genomics?
Oracle Genomics is South Africa’s trusted partner for genetic testing, with:
- Nationwide Coverage: Serving patients in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Our tests are supervised by qualified general physicians
- Advanced Technology: Using NGS technology for 99.9% accuracy
- Patient-Centred Care: We understand the emotional journey of genetic testing
- Complete Support: From initial counselling to results explanation
We’ve helped thousands of South Africans gain clarity about their genetic health, and we’re here to support you through every step of this important journey.
Take the First Step Toward Clarity
Don’t let uncertainty about cerebral cavernous malformations control your life. With our special pricing of ZAR 6,700, now is the perfect time to gain the knowledge that could protect your neurological health for years to come.
Book your test today and receive:
- Priority scheduling for faster results
- Convenient sample collection options (blood, extracted DNA, or FTA card)
- Professional genetic counselling included
- Peace of mind that comes from definitive answers
Contact us now to schedule your genetic counselling session and begin your journey to better health understanding. Our team is ready to provide the compassionate, professional care you deserve.
