Understanding Your Child’s Seizures: Finding Answers Through Genetic Testing
As a parent, watching your infant experience unexplained seizures can be one of the most frightening experiences imaginable. The uncertainty, the hospital visits, the endless questions – we understand the emotional toll this takes on South African families. Our PCDH19 Gene Test is designed to provide the clarity and answers you desperately need during this challenging time.
What Does This Test Detect?
This advanced genetic test specifically identifies mutations in the PCDH19 gene, which are responsible for Early Infantile Epileptic Encephalopathy Type 9. Using cutting-edge Next-Generation Sequencing (NGS) technology, we examine your child’s DNA with exceptional accuracy to detect even the smallest genetic variations that could be causing their neurological symptoms.
Who Should Consider This Test?
This test is essential for infants and young children experiencing:
- Unexplained seizures or epilepsy starting in infancy
- Developmental delays or regression following seizure onset
- Clusters of seizures occurring close together
- Family history of similar neurological conditions
- Female children with seizure disorders (PCDH19 mutations often affect females more severely)
Why Early Detection Matters for Your Child’s Health
Getting an accurate diagnosis through genetic testing can transform your child’s healthcare journey. With a confirmed PCDH19 diagnosis, your medical team can:
- Develop targeted treatment strategies specific to this genetic condition
- Provide accurate prognosis information for future planning
- Offer appropriate genetic counselling for family planning decisions
- Connect you with support networks and resources for PCDH19 families
- Reduce the diagnostic odyssey and unnecessary medical testing
Understanding Your Results: Clear Guidance Every Step
We know that waiting for genetic test results can be anxiety-provoking. That’s why we provide comprehensive support throughout the process. Your results will include:
- Clear explanation of any PCDH19 gene mutations detected
- Detailed report explaining what the findings mean for your child
- Access to genetic counselling to help interpret results
- Guidance on next steps and available treatment options
- Support in communicating results to your healthcare team
Transparent Pricing – Exceptional Value for Peace of Mind
| Service | Regular Price | Special Price |
|---|---|---|
| PCDH19 Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | INCLUDED | |
| Family Pedigree Analysis | INCLUDED | |
| Results Interpretation | INCLUDED | |
Considering the potential savings from avoiding unnecessary treatments and tests, this investment in your child’s health provides exceptional long-term value.
Nationwide Trust and Accessibility
Oracle Genomics brings world-class genetic testing to families across South Africa. With testing facilities in Johannesburg, Cape Town, Durban, and Pretoria, we ensure that every South African family has access to the advanced medical technology they deserve. Our team of neurologists and genetic specialists work together to provide the comprehensive care your family needs.
Take the First Step Toward Answers
Don’t let uncertainty about your child’s health continue to cause anxiety. Early detection through genetic testing can provide the answers you need to make informed decisions about their care. Our simple testing process requires only a blood sample or DNA extraction, and we guide you through every step with compassion and professionalism.
Book your PCDH19 Gene Test today and take control of your child’s neurological health journey. Call us now or visit our website to schedule your test and genetic counselling session. Your child’s future health deserves the clarity that only accurate genetic testing can provide.
