Find Answers for Your Infant’s Unexplained Seizures
When your baby experiences seizures that don’t have a clear cause, the uncertainty can be overwhelming. As parents, you deserve answers and a clear path forward. Our GABRA1 Gene Early Infantile Epileptic Encephalopathy Type 19 NGS Genetic DNA Test provides the medical clarity you need to understand your child’s condition and make informed treatment decisions.
Understanding the GABRA1 Epilepsy Genetic Test
The GABRA1 gene plays a crucial role in brain function, specifically in controlling electrical activity that prevents seizures. When this gene has mutations, it can lead to Early Infantile Epileptic Encephalopathy Type 19 – a severe form of epilepsy that typically appears in the first months of life. Our advanced Next-Generation Sequencing (NGS) technology examines this gene with exceptional accuracy, identifying even the smallest genetic variations that could be causing your infant’s symptoms.
This isn’t just another test – it’s a comprehensive genetic investigation that provides definitive answers about whether your child’s seizures have a genetic basis. The results can guide treatment decisions, help predict disease progression, and provide crucial information for family planning.
Is This Test Right for Your Family?
This test is specifically designed for infants and families experiencing:
- Unexplained seizures starting in the first year of life
- Multiple seizure types that are difficult to control with medication
- Developmental delays or regression following seizure onset
- Family history of epilepsy or seizure disorders
- Abnormal EEG patterns without clear structural brain abnormalities
- Concerns about genetic conditions affecting brain development
If your infant has been diagnosed with epilepsy or shows seizure-like activity, this test could provide the missing piece to understanding their condition.
Why Early Detection Matters for Your Child’s Future
Getting a genetic diagnosis for your infant’s epilepsy isn’t just about having a label – it’s about opening doors to better care and improved outcomes:
- Personalised Treatment Plans: Genetic results can guide medication choices and help avoid ineffective treatments
- Developmental Support: Early intervention with appropriate therapies can improve long-term development
- Family Planning Guidance: Understand recurrence risks for future pregnancies
- Reduced Diagnostic Uncertainty: End the cycle of endless testing and uncertainty
- Connection to Specialist Care: Genetic diagnosis can facilitate access to epilepsy specialists and support services
Every day without answers is a day without the most appropriate care for your child. Early genetic testing can make a significant difference in their developmental trajectory.
Understanding Your Test Results – Clear Guidance Every Step
We understand that genetic test results can be confusing and anxiety-provoking. That’s why we provide comprehensive support:
- Clear, Easy-to-Understand Reports: Your results will be explained in plain language with clinical significance clearly outlined
- Genetic Counselling Session: Included with your test to help you understand the implications for your child and family
- Clinical Correlation: Our neurologists help interpret how the genetic findings relate to your child’s symptoms
- Next Steps Guidance: Practical recommendations for treatment, monitoring, and specialist referrals
- Ongoing Support: Access to our team for any follow-up questions about your results
You won’t be left to interpret complex genetic information alone – we’re here to guide you through every step.
Transparent Pricing – Exceptional Value for Peace of Mind
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| GABRA1 Genetic Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | INCLUDED | ||
| Clinical Interpretation | INCLUDED | ||
| Results Support | INCLUDED | ||
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Consider the value: Early diagnosis could prevent years of ineffective treatments, unnecessary hospital visits, and developmental challenges. This investment in your child’s health could save significantly on long-term healthcare costs.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Serving families across South Africa including Johannesburg, Cape Town, Durban, Pretoria and beyond
- Expert Neurologist Oversight: All tests are supervised by qualified neurologists specialising in epilepsy genetics
- Cutting-Edge NGS Technology: Most advanced genetic testing available with exceptional accuracy
- Comprehensive Preparation: Includes genetic counselling and family history assessment
- Proven Track Record: Trusted by healthcare providers across South Africa
- Patient-First Approach: We understand the emotional journey of parents facing childhood epilepsy
Take the First Step Toward Answers Today
Don’t let uncertainty about your infant’s seizures continue to cause stress and worry. Every day without answers delays the most appropriate care for your child.
Limited Time Special Pricing: Save ZAR 2,650 while this offer lasts
Rapid Results: Get answers in 3-4 weeks, not months
Convenient Sampling: Multiple sample options to suit your family’s needs
Your child’s developmental future is too important to wait. Contact Oracle Genomics today and take the first step toward understanding and managing your infant’s epilepsy with confidence.
