Understanding SRPX2 Gene-Related Neurological Conditions
When your child or family member experiences seizures, developmental delays, or speech difficulties, the uncertainty can be overwhelming. The SRPX2 Gene Test offers clarity and direction for families navigating these complex neurological challenges. This comprehensive genetic analysis specifically targets the SRPX2 gene mutations linked to Rolandic epilepsy, intellectual disability, and speech coordination disorders.
What Does This Test Detect?
Our advanced Next Generation Sequencing (NGS) technology examines the SRPX2 gene for specific mutations known to cause:
- Rolandic epilepsy (benign childhood epilepsy with centrotemporal spikes)
- Intellectual disability and developmental delays
- Speech dyspraxia (difficulty coordinating speech movements)
- Potential inheritance patterns within families
Who Should Consider This Genetic Test?
This test is particularly important if you or your child experiences:
- Focal seizures, especially during sleep or upon waking
- Speech difficulties or delayed language development
- Learning challenges or intellectual disability
- Family history of epilepsy or developmental disorders
- Unexplained neurological symptoms in childhood
- Concerns about genetic inheritance for family planning
Why Early Genetic Diagnosis Matters
Receiving a definitive genetic diagnosis provides numerous benefits for your family’s health journey:
- Personalised Treatment Plans: Guide medication choices and therapeutic interventions
- Family Planning Insights: Understand inheritance risks for future children
- Reduced Diagnostic Uncertainty: End the cycle of multiple specialist visits
- Educational Support: Access appropriate school accommodations and resources
- Emotional Peace: Replace uncertainty with understanding and control
Understanding Your Test Results
Our comprehensive genetic counselling ensures you fully understand your results. We provide:
- Clear explanation of genetic findings in plain language
- Discussion of what results mean for treatment and management
- Family pedigree analysis to understand inheritance patterns
- Guidance on next steps and specialist referrals
- Ongoing support for questions and concerns
Comprehensive Pricing & Value
| Service | Regular Price | Special Price |
|---|---|---|
| SRPX2 Gene NGS Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Result Explanation | Included | |
Consider the long-term value: Early genetic diagnosis can prevent years of unnecessary treatments, reduce hospital visits, and provide targeted interventions that significantly improve quality of life.
Why Trust Oracle Genomics?
We understand the emotional weight of genetic testing for neurological conditions. That’s why we’ve built our service around:
- Medical Expertise: Specialist neurologists and genetic counsellors
- Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
- Nationwide Accessibility: Testing available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Multiple Sample Options: Blood draw, extracted DNA, or simple FTA card collection
- Fast Turnaround: Results typically within 3-4 weeks
- Complete Support: From initial consultation to result understanding
Take the First Step Toward Clarity
Don’t let uncertainty about neurological symptoms control your family’s future. Our SRPX2 Gene Test provides the answers you need to make informed healthcare decisions and access appropriate support services.
Book Your Genetic Consultation Today:
Call our specialist team or complete our online booking form. We’ll guide you through the simple process and answer any questions about testing, preparation, or what to expect.
Early genetic diagnosis can transform uncertainty into understanding. Take control of your neurological health journey with confidence and clarity.
