Understanding Your Infant’s Seizures: The SCN1A Gene Test
As a parent, watching your infant experience seizures can be terrifying and overwhelming. You’re searching for answers, for clarity, for a way to help your child. The SCN1A Gene Early Infantile Epileptic Encephalopathy Type 6 NGS Genetic DNA Test is designed to provide the definitive answers you need during this difficult time.
What This Test Detects
This advanced genetic test specifically identifies mutations in the SCN1A gene, which is responsible for producing a protein crucial for proper brain function. When this gene is mutated, it can cause Early Infantile Epileptic Encephalopathy Type 6 (EIEE6), a severe form of epilepsy that typically begins in the first year of life. Our NGS (Next-Generation Sequencing) technology examines every part of the SCN1A gene with exceptional precision, ensuring no mutation goes undetected.
Who Should Consider This Test
This test is essential for infants and young children experiencing:
- Frequent seizures that began in infancy
- Developmental delays or regression
- Abnormal EEG patterns
- Family history of epilepsy or neurological disorders
- Resistance to standard anti-epileptic medications
- Unexplained neurological symptoms
Why Early Detection Matters for Your Child’s Health
Early diagnosis of SCN1A-related epilepsy can be life-changing for your child. With accurate genetic confirmation, your neurologist can:
- Prescribe targeted treatments that are more effective
- Avoid medications that may worsen the condition
- Develop a comprehensive management plan
- Provide accurate prognosis and expectations
- Offer genetic counselling for family planning
Understanding Your Results
We understand that waiting for genetic test results can be anxiety-provoking. Our team provides clear, compassionate explanations of your results, including:
- Detailed report of any SCN1A gene mutations found
- Explanation of what the results mean for your child’s health
- Guidance on next steps and treatment options
- Access to genetic counselling services
- Support in communicating results to your healthcare team
Transparent Pricing – ZAR
| Service | Price |
|---|---|
| Regular Price | ZAR 9,350 |
| Special Price | ZAR 6,700 |
| Turnaround Time | 3-4 Weeks |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card |
Nationwide Coverage Across South Africa
We make genetic testing accessible to families across South Africa. Our services are available in:
- Johannesburg and surrounding areas
- Cape Town and Western Cape region
- Durban and KwaZulu-Natal
- Pretoria and Gauteng province
- Plus nationwide coverage through our partner network
Take Action for Your Child’s Health Today
Don’t let uncertainty about your infant’s seizures continue to cause stress and worry. Early detection through genetic testing can provide the answers you need to make informed decisions about your child’s care. Our team of neurological genetics specialists is ready to support your family with:
- Comprehensive pre-test genetic counselling
- Accurate, reliable testing with 99.9% accuracy
- Clear, compassionate result explanations
- Ongoing support and guidance
Book your consultation today and take the first step toward understanding your child’s condition. Early detection leads to better outcomes – don’t wait to get the answers your family deserves.
