Finding Answers for Your Child’s Neurological Health
As a parent, watching your infant struggle with seizures or developmental delays can be heartbreaking and overwhelming. You’re not alone in seeking answers, and we’re here to provide the clarity you need through advanced genetic testing specifically designed for early infantile epileptic encephalopathy.
Understanding the FGF12 Gene Test
The FGF12 Gene Early Infantile Epileptic Encephalopathy Type 47 test uses cutting-edge Next-Generation Sequencing (NGS) technology to examine the FGF12 gene for mutations that cause this severe form of epilepsy. This isn’t just another test – it’s a comprehensive diagnostic tool that can provide life-changing answers for your family.
When the FGF12 gene doesn’t function properly, it can disrupt normal brain development and electrical activity, leading to the seizures and developmental challenges characteristic of this condition. Our test specifically looks for these genetic variations with exceptional accuracy.
Who Should Consider This Test?
This test is particularly important if your infant shows any of these symptoms:
- Early-onset seizures (typically beginning in the first months of life)
- Developmental regression or delays in milestones
- Abnormal brain activity patterns detected through EEG
- Family history of early infantile epilepsy or neurological disorders
- Unexplained developmental concerns despite normal initial assessments
If you’ve been searching for answers while watching your child struggle, this test could provide the clarity needed to move forward with appropriate care and treatment.
Why Early Detection Matters for Your Child’s Future
Getting an accurate diagnosis through genetic testing offers multiple life-changing benefits:
- Personalised Treatment Plans: Knowing the specific genetic cause allows neurologists to tailor treatments that may be more effective for your child’s unique condition
- Family Planning Guidance: Understand the inheritance pattern and risks for future pregnancies
- Early Intervention: Begin appropriate therapies and interventions sooner, potentially improving long-term outcomes
- Peace of Mind: End the diagnostic odyssey and uncertainty that often accompanies rare neurological conditions
- Connection to Support: Connect with other families facing similar challenges and access specialised resources
Understanding Your Results with Compassion
We know that waiting for genetic test results can be an anxious time. That’s why we provide comprehensive support throughout the process:
- Clear, Understandable Reports: Your results will be explained in plain language, with detailed guidance on what they mean for your child’s health
- Genetic Counselling Included: Every test includes a session with our qualified genetic counsellors who will help you understand the implications and next steps
- Family Pedigree Analysis: We’ll help map your family history to better understand inheritance patterns
- Neurologist Collaboration: We work closely with South Africa’s leading neurologists to ensure coordinated care
Whether the results provide a clear diagnosis or rule out this specific condition, you’ll have the information needed to make informed decisions about your child’s care.
Transparent Pricing for South African Families
| Service | Regular Price | Special Price |
|---|---|---|
| FGF12 Gene Test (NGS Technology) | ZAR 6,700 | |
| Genetic Counselling Session | INCLUDED | |
| Family Pedigree Analysis | INCLUDED | |
| Results Interpretation | INCLUDED | |
| Turnaround Time | 3-4 Weeks | |
Considering the potential lifetime costs of undiagnosed neurological conditions and the value of early intervention, this test represents significant long-term health savings and peace of mind.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing services across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria
- Advanced NGS Technology: Using the same cutting-edge genetic sequencing technology trusted by leading medical institutions worldwide
- Specialised Neurological Expertise: Tests developed and interpreted in collaboration with specialist neurologists
- Comprehensive Support: From sample collection to results explanation, we’re with you every step of the way
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card for your convenience
Take the First Step Toward Answers Today
Don’t let uncertainty about your child’s neurological health continue to cause worry and stress. Early detection through genetic testing can provide the answers you need to move forward with confidence.
Book Your Test Now: Call us directly at [INSERT PHONE] or visit our website to schedule your genetic counselling session and testing.
Convenient Locations: Available at medical centres throughout Johannesburg, Cape Town, Durban, Pretoria and nationwide.
Urgent Note: The sooner you have answers, the sooner you can access appropriate treatments and support for your child. Every day matters when it comes to early intervention for neurological conditions.
