Finding Answers for Your Child’s Unexplained Seizures
When your child experiences seizures that don’t respond to standard treatments, the uncertainty can be overwhelming. The CHD2 Gene Epileptic Encephalopathy test provides the clarity you need to understand your child’s condition and make informed treatment decisions. This specialised genetic test identifies mutations that cause severe childhood epilepsy, helping you and your healthcare team develop the most effective care plan.
Understanding the CHD2 Gene Test
The CHD2 gene plays a crucial role in brain development and function. When mutations occur in this gene, they can cause epileptic encephalopathy – a severe form of epilepsy that typically begins in early childhood (1-4 years). Our Next Generation Sequencing (NGS) technology examines the CHD2 gene with exceptional precision, identifying even the smallest genetic variations that might be causing your child’s seizures.
This isn’t just another epilepsy test – it’s a targeted investigation into one of the specific genetic causes of childhood epilepsy, providing answers when other tests have failed to explain your child’s symptoms.
Who Should Consider This Test?
This test is particularly important for children who experience:
- Unexplained seizures beginning in early childhood (1-4 years)
- Multiple seizure types that are difficult to control with medication
- Developmental delays or regression following seizure onset
- Abnormal EEG patterns without clear cause
- Family history of epilepsy or developmental disorders
- Seizures accompanied by behavioural changes or cognitive decline
If your child’s epilepsy hasn’t responded well to standard treatments, or if you’ve been searching for answers without success, this test could provide the breakthrough you need.
Why Early Detection Matters for Your Child’s Health
Identifying a CHD2 gene mutation early can significantly impact your child’s quality of life and treatment outcomes:
- Personalised Treatment: Knowing the genetic cause helps neurologists select the most effective anti-epileptic medications
- Better Seizure Control: Targeted treatments can reduce seizure frequency and severity
- Developmental Support: Early intervention can help address developmental delays more effectively
- Family Planning: Understanding the genetic basis helps with future family planning decisions
- Reduced Hospitalisations: Better seizure management means fewer emergency visits
Every day without answers can mean more seizures and developmental challenges. Early detection gives your child the best chance for improved outcomes.
Understanding Your Test Results
We know waiting for genetic test results can be anxiety-provoking. Our process is designed to be as clear and supportive as possible:
- Comprehensive Report: You’ll receive a detailed report explaining any CHD2 gene mutations found
- Genetic Counselling: Included with your test, our genetic counsellors help you understand what the results mean for your child
- Clinical Guidance: The report provides specific information to share with your neurologist for treatment planning
- Family Implications: We explain what the results might mean for other family members
- Ongoing Support: We’re here to answer questions throughout the process
Whether the test identifies a mutation or provides reassurance by ruling out CHD2-related epilepsy, you’ll have the information needed to move forward with confidence.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| CHD2 Gene Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling | Included at no extra cost | ||
| Results Interpretation | Included at no extra cost | ||
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Consider the value: Early diagnosis can prevent years of ineffective treatments, unnecessary medications, and repeated hospital visits – potentially saving thousands in healthcare costs while improving your child’s quality of life.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests reviewed by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS technology with 99.9% accuracy
- Certified Laboratories: All testing performed in SANAS-accredited facilities
- Patient-Focused Care: We understand the emotional journey of genetic testing
- Comprehensive Support: From sample collection to results explanation
Take the First Step Toward Answers Today
Don’t let uncertainty about your child’s seizures continue. Every day without answers can impact their development and quality of life. Our special pricing of ZAR 6,700 makes this crucial testing accessible to South African families.
Preparation Required: Please bring your child’s clinical history and be prepared for a genetic counselling session to create a family pedigree chart. This helps us provide the most comprehensive analysis possible.
Early detection leads to better outcomes. The sooner we identify the cause of your child’s seizures, the sooner we can help implement effective treatments. Contact us today to schedule your CHD2 gene test and start your journey toward answers and improved seizure management.
