Find Clarity About Vanishing White Matter Disease
When neurological symptoms appear or family history raises concerns, the uncertainty can be overwhelming. Our EIF2B3 Gene Leukoencephalopathy test provides the answers South African families need to understand their genetic risk and take control of their neurological health.
Understanding Your EIF2B3 Genetic Test
This specialised test examines the EIF2B3 gene using advanced Next Generation Sequencing (NGS) technology to identify mutations that cause leukoencephalopathy with vanishing white matter. This rare neurological condition affects the brain’s white matter, leading to progressive neurological symptoms. Our test provides the most accurate detection available, giving you and your healthcare provider the information needed for proper diagnosis and management.
Who Should Consider This Genetic Test?
- Individuals experiencing unexplained neurological symptoms like coordination difficulties, muscle weakness, or cognitive changes
- Children or adults with suspected white matter abnormalities on brain imaging
- Those with a family history of leukoencephalopathy or vanishing white matter disease
- Parents concerned about genetic risks for their children’s neurological health
- Patients undergoing neurological evaluation for unexplained symptoms
Why Early Detection Matters for Your Health
Identifying EIF2B3 gene mutations early can significantly impact your health journey. Early detection allows for:
- Accurate diagnosis and appropriate medical management
- Better understanding of disease progression and prognosis
- Informed family planning decisions
- Access to specialised neurological care and support
- Peace of mind through genetic counselling and personalised guidance
Understanding Your Test Results
Our genetic counsellors will help you understand your results in clear, compassionate terms. We provide:
- Detailed explanation of any detected EIF2B3 gene mutations
- Information about what the results mean for your health
- Guidance on next steps and available treatment options
- Support for discussing results with family members
- Connection to neurological specialists if needed
Remember: A positive result doesn’t necessarily mean you’ll develop symptoms, and our team is here to support you every step of the way.
Affordable Genetic Testing for South African Families
| Test Feature | Details | Cost |
|---|---|---|
| Regular Price | Comprehensive EIF2B3 gene analysis | ZAR 9,350 |
| Special Price | Limited time offer | ZAR 6,700 |
| Turnaround Time | Results in 3-4 weeks | Included |
| Genetic Counselling | Pre- and post-test sessions | Included |
Compared to the potential costs of undiagnosed neurological conditions, this test represents excellent value for your health investment.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS technology for maximum accuracy
- Patient-Centred Care: Empathetic support throughout your testing journey
- Proven Reliability: Trusted by healthcare professionals across South Africa
Take the First Step Toward Neurological Health Clarity
Don’t let uncertainty about genetic risks affect your peace of mind. Our EIF2B3 Gene Leukoencephalopathy test provides the answers you need to make informed health decisions.
Limited Time Special: Book now to secure your test at the special price of ZAR 6,700 – saving you ZAR 2,650 off the regular price.
Early detection of neurological conditions can significantly improve management outcomes. Don’t delay – take control of your genetic health today.
Simple Sample Collection
We make testing convenient with multiple sample options: Blood draw, Extracted DNA, or Simple finger-prick blood spot on FTA card. Our trained professionals ensure comfortable collection at locations throughout South Africa.
