Find Answers for Your Infant’s Unexplained Seizures
When your baby experiences seizures that don’t respond to standard treatments, the uncertainty can be overwhelming. Our DOCK7 Gene Early Infantile Epileptic Encephalopathy Type 23 test provides the clarity you need to make informed decisions about your child’s care and future.
Understanding the DOCK7 Gene Test
This specialised genetic test examines the DOCK7 gene using Next-Generation Sequencing (NGS) technology to identify mutations that cause Early Infantile Epileptic Encephalopathy Type 23. This is a severe form of epilepsy that typically begins in the first months of life and can significantly impact neurological development.
Unlike standard epilepsy tests, our analysis provides specific genetic information that can help neurologists develop more targeted treatment approaches and understand the long-term prognosis for your child.
Who Should Consider This Test?
This test is particularly important for infants and families experiencing:
- Unexplained seizures beginning in early infancy (first 3-6 months)
- Seizures that don’t respond well to standard anti-epileptic medications
- Developmental delays or regression following seizure onset
- Abnormal EEG patterns consistent with epileptic encephalopathy
- Family history of similar neurological conditions
- Multiple seizure types that are difficult to control
If your child’s condition has been difficult to diagnose or treat effectively, this genetic insight could be the breakthrough you need.
Why Early Detection Matters for Your Child’s Health
Getting a definitive diagnosis through genetic testing provides several crucial benefits:
- Personalised Treatment: Specific genetic information helps neurologists choose the most effective medications and therapies
- Prognostic Clarity: Understand the likely progression and long-term outcomes
- Family Planning: Make informed decisions about future pregnancies
- Early Intervention: Begin appropriate therapies and support services sooner
- Reduced Diagnostic Odyssey: Avoid years of uncertainty and multiple specialist visits
- Peace of Mind: Replace uncertainty with understanding and a clear care plan
Understanding Your Test Results
We know waiting for genetic test results can be anxiety-provoking. Our process is designed to provide clarity and support:
- Clear Reporting: Results are presented in easy-to-understand language with medical interpretation
- Genetic Counselling: Included session to explain findings and implications
- Family Pedigree: We help create a detailed family history chart
- Next Steps Guidance: Clear recommendations for follow-up care and specialist referrals
- Ongoing Support: Access to our team for any additional questions
Whether the results confirm DOCK7-related epilepsy or rule it out, you’ll have valuable information to guide your child’s care journey.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| DOCK7 Gene Test | ZAR 6,700 | ZAR 2,650 | |
| Genetic Counselling | Included at no extra cost | ||
| Family Pedigree Analysis | Included at no extra cost | ||
| Results Interpretation | Included at no extra cost | ||
Consider the value: Early diagnosis can prevent years of unnecessary treatments and specialist visits, potentially saving tens of thousands in medical costs.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
- Rapid Turnaround: Results in 3-4 weeks – faster than many international labs
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Comprehensive Support: From initial consultation through results interpretation
Take the First Step Toward Answers Today
Don’t let uncertainty about your child’s condition continue. Every day without a clear diagnosis delays appropriate care and adds to family stress.
Why act now?
- Early intervention during critical developmental windows can improve outcomes
- Reduce the emotional toll of not knowing what’s causing your child’s symptoms
- Special pricing of ZAR 6,700 represents significant savings
- Begin the journey toward targeted, effective treatment
Your child’s neurological health is too important to wait. Contact Oracle Genomics today and start the journey toward understanding and effective care.
