Find Answers for Your Infant’s Seizures with SCN8A Gene Testing
When your precious baby experiences unexplained seizures or developmental delays, the uncertainty can be overwhelming. Every parent deserves clear answers and a path forward. Our SCN8A Gene Early Infantile Epileptic Encephalopathy Type 13 test provides the definitive genetic diagnosis that can transform your child’s treatment journey and future outcomes.
Understanding the SCN8A Gene Test
The SCN8A gene plays a crucial role in brain function, and mutations in this gene can cause Early Infantile Epileptic Encephalopathy Type 13 – a severe form of epilepsy that begins in infancy. Our Next-Generation Sequencing (NGS) technology examines this specific gene with exceptional accuracy, identifying the exact genetic variations that may be causing your child’s symptoms.
This isn’t just another test – it’s a comprehensive diagnostic tool that provides the clarity needed for targeted treatment approaches. By understanding the genetic basis of your child’s condition, healthcare providers can develop more effective management strategies.
Who Should Consider This Test?
This test is essential for infants and young children experiencing:
- Unexplained seizures beginning in early infancy
- Developmental delays or regression
- Movement disorders or abnormal muscle tone
- Family history of epilepsy or neurological conditions
- Resistance to standard anti-epileptic medications
- Multiple seizure types that are difficult to control
If your child’s symptoms match these descriptions, genetic testing could provide the breakthrough answers you’ve been seeking.
Why Early Detection Matters for Your Child’s Health
Early genetic diagnosis through SCN8A testing offers life-changing benefits:
- Personalised Treatment: Identify the most effective anti-epileptic medications for your child’s specific genetic profile
- Proactive Management: Implement targeted interventions before irreversible neurological damage occurs
- Family Planning: Understand inheritance patterns for future family planning decisions
- Reduced Hospitalisations: Better seizure control means fewer emergency room visits
- Peace of Mind: Replace uncertainty with a clear diagnosis and treatment pathway
Understanding Your Test Results
We understand that waiting for genetic test results can be anxiety-provoking. Our comprehensive approach includes:
- Clear Interpretation: Results presented in easy-to-understand language with medical guidance
- Genetic Counselling: Included session to help you understand the implications for your family
- Clinical Correlation: Expert analysis connecting genetic findings to your child’s symptoms
- Next Steps Guidance: Clear recommendations for treatment and specialist referrals
- Ongoing Support: Access to our team for any follow-up questions or concerns
Remember: A positive result means we’ve found the cause, opening doors to targeted treatment. A negative result helps rule out this specific condition, allowing focus on other diagnostic possibilities.
Affordable, Life-Changing Genetic Testing
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| SCN8A Gene Test | ZAR 6,700 | ZAR 2,650 |
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Preparation: Clinical history and genetic counselling session included
Consider this investment in your child’s health: Early diagnosis can prevent years of unnecessary treatments and hospital visits, potentially saving thousands in medical costs while improving quality of life.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing across South Africa, including Johannesburg, Cape Town, Durban, Pretoria and surrounding areas
- Medical Expertise: Specialist neurologist oversight ensuring clinical accuracy
- Advanced Technology: State-of-the-art NGS methodology for reliable results
- Genetic Counselling: Professional guidance included with every test
- Proven Accuracy: Rigorous quality control measures for peace of mind
- South African Focus: Understanding of local healthcare needs and challenges
Take the First Step Toward Answers Today
Don’t let uncertainty about your child’s health continue. Every day without a clear diagnosis means delayed intervention and unnecessary suffering.
Book your SCN8A gene test now and get:
- Definitive answers about your child’s condition
- Personalised treatment recommendations
- Professional genetic counselling session
- Special pricing at ZAR 6,700 (save ZAR 2,650)
- Nationwide accessibility across South Africa
Limited time special pricing available. Early detection can make all the difference in your child’s developmental journey.
Act Now: The window for optimal intervention in early infantile epilepsy is limited. Early genetic diagnosis provides the foundation for effective treatment strategies that can significantly improve long-term outcomes.
