Understanding CTNNA2 Gene Testing: Your Path to Neurological Health Clarity
When you’re concerned about neurological development or have a family history of brain disorders, the uncertainty can feel overwhelming. Our CTNNA2 Gene Neuronal Migration Disorder NGS Genetic DNA Test provides the answers you need with compassion and medical excellence. For ZAR 6,700, gain access to cutting-edge genetic technology that could transform your understanding of neurological health.
What Does This Test Detect?
The CTNNA2 gene plays a vital role in brain development, specifically in how nerve cells (neurons) migrate to their proper positions during fetal development. When this gene has mutations, it can lead to neuronal migration disorders that may cause developmental delays, epilepsy, or other neurological conditions. Our Next Generation Sequencing (NGS) technology examines this gene with exceptional accuracy, providing you with reliable results you can trust for making informed healthcare decisions.
Who Should Consider This Test?
This test is particularly important if you or your loved one experiences:
- Unexplained developmental delays in childhood
- Family history of neurological disorders
- Diagnosed epilepsy with unknown cause
- Abnormal brain development findings on scans
- Planning pregnancy with family neurological history
Many South African families find peace of mind through genetic clarity, especially when facing complex neurological concerns.
Why Early Detection Matters for Your Health
Identifying CTNNA2 gene mutations early can significantly impact treatment approaches and family planning decisions. Benefits include:
- Personalised Treatment Plans: Guide neurologists in creating targeted interventions
- Family Planning Confidence: Make informed decisions about future pregnancies
- Reduced Diagnostic Uncertainty: End the cycle of unexplained symptoms
- Proactive Health Management: Implement early interventions when most effective
- Peace of Mind: Replace uncertainty with clear understanding
Understanding Your Results with Compassion
We understand that genetic testing can feel daunting. That’s why we provide comprehensive support throughout your journey:
- Clear Explanations: Results presented in easy-to-understand language
- Genetic Counselling: Professional guidance to interpret findings
- Family History Analysis: Creating pedigree charts to understand inheritance patterns
- Next Steps Guidance: Clear recommendations for follow-up care
- Ongoing Support: Access to our neurological genetics specialists
Your results will be available within 3-4 weeks, and we’ll be with you every step of the way.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| CTNNA2 Gene Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | INCLUDED | ||
| Family Pedigree Analysis | INCLUDED | ||
| Results Interpretation | INCLUDED | ||
Consider the long-term value: Early detection can prevent years of unnecessary treatments and provide clarity that impacts generations.
Why Trust Oracle Genomics?
We’ve built our reputation on medical excellence and patient care:
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Specialised neurological genetics team
- Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Comprehensive Preparation: Clinical history review and genetic counselling included
- Proven Track Record: Trusted by neurologists nationwide
Take the First Step Toward Clarity Today
Don’t let uncertainty about neurological health continue to cause anxiety. Our compassionate team is ready to guide you through this important journey.
Early detection saves time, reduces uncertainty, and provides the clarity needed for effective treatment planning. Don’t wait – take control of your neurological health today.
