Understanding Your Child’s Seizures: GABRB3 Gene Epilepsy Testing
When your child experiences those brief staring spells or sudden lapses in awareness, it’s natural to feel concerned and uncertain. Childhood absence epilepsy can be confusing and frightening for parents, but understanding the genetic basis can bring clarity and direction. Our GABRB3 Gene Epilepsy Test provides the answers you need to make informed decisions about your child’s health journey.
What This Test Reveals About Your Child’s Health
The GABRB3 gene plays a crucial role in brain function, specifically in regulating electrical activity that prevents seizures. When mutations occur in this gene, it can lead to childhood absence epilepsy type 5 – characterized by brief episodes where your child seems to “space out” or stare blankly. Our advanced Next-Generation Sequencing (NGS) technology examines this gene with exceptional accuracy, identifying the specific genetic variations that may be causing these episodes.
Is This Test Right for Your Family?
Consider this test if your child experiences:
- Brief staring spells lasting 10-20 seconds
- Sudden cessation of activity mid-sentence
- Repetitive blinking or mouth movements during episodes
- Quick return to normal activity with no memory of the event
- Family history of epilepsy or seizure disorders
Early genetic identification can help prevent academic struggles, social challenges, and potential injury risks associated with undiagnosed absence seizures.
Why Genetic Testing Matters for Childhood Epilepsy
Getting a definitive genetic diagnosis provides multiple benefits:
- Targeted Treatment: Specific anti-epileptic medications work better for absence seizures
- Family Planning: Understand inheritance patterns for future children
- Academic Support: Help schools provide appropriate accommodations
- Peace of Mind: Replace uncertainty with clear understanding
- Proactive Management: Monitor and manage condition effectively
Understanding Your Test Results
We make complex genetic information accessible and understandable:
- Positive Result: Identifies a GABRB3 gene mutation – our genetic counsellors will explain what this means for treatment and family planning
- Negative Result: No mutation detected – provides reassurance and may guide investigation of other causes
- Variant of Uncertain Significance: Rare finding requiring further evaluation – we provide complete guidance
Every result includes a comprehensive genetic counselling session to ensure you fully understand the implications and next steps.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| GABRB3 Gene Epilepsy Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | INCLUDED | ||
| Family Pedigree Analysis | INCLUDED | ||
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Serving families in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
- Complete Support: Genetic counselling included with every test
- Proven Reliability: Trusted by healthcare professionals nationwide
Take the First Step Toward Understanding
Don’t let uncertainty about your child’s health continue. Early detection through genetic testing can make a significant difference in treatment outcomes and quality of life.
Limited Time Offer: Save ZAR 2,650 on comprehensive GABRB3 epilepsy testing. Early diagnosis leads to better management outcomes.
