Find Answers for Your Infant’s Neurological Health
When your baby experiences unexplained seizures or developmental delays, the uncertainty can be overwhelming. Our ARHGEF9 Gene Early Infantile Epileptic Encephalopathy Type 8 NGS Genetic DNA Test provides the clarity and answers you desperately need. For just ZAR 6,700, you can access cutting-edge genetic testing that helps identify the root cause of early-onset epilepsy, giving you the power to make informed decisions about your child’s healthcare journey.
Understanding the ARHGEF9 Epilepsy DNA Test
This specialised genetic test examines the ARHGEF9 gene using advanced Next-Generation Sequencing (NGS) technology. The ARHGEF9 gene plays a crucial role in brain development and function, and mutations in this gene can lead to Early Infantile Epileptic Encephalopathy Type 8 – a severe form of epilepsy that typically appears in the first months of life. Our test provides comprehensive analysis to detect these genetic variations, helping healthcare providers develop targeted treatment strategies.
Who Should Consider This Test?
This test is particularly important for families where:
- Infants experience unexplained seizures within the first year of life
- There’s a family history of early-onset epilepsy or developmental delays
- Your child shows developmental regression or slowed milestones
- Standard epilepsy treatments haven’t been effective
- You’re planning another pregnancy and want to understand genetic risks
Early detection can significantly impact treatment outcomes and quality of life.
Why Early Detection Matters for Your Child’s Health
Getting answers early can transform your child’s healthcare journey. Benefits include:
- Personalised Treatment: Results can guide more effective medication choices
- Developmental Planning: Early intervention for better developmental outcomes
- Family Planning: Understanding genetic risks for future pregnancies
- Peace of Mind: Reducing the uncertainty and stress of unexplained symptoms
- Better Management: Creating targeted care plans with your neurologist
Understanding Your Results with Compassion
We understand that genetic testing can be anxiety-provoking. That’s why our process includes:
- Professional Genetic Counselling: Before testing, you’ll meet with our genetic counsellor to create a family pedigree and discuss what to expect
- Clear Result Interpretation: Your results will be explained in straightforward language
- Ongoing Support: We provide guidance on next steps and connecting with appropriate specialists
- 3-4 Week Turnaround: Quick results mean faster answers and earlier interventions
Affordable, Accessible Genetic Testing
| Test Option | Price | Value |
|---|---|---|
| Regular Price | ZAR 9,350 | Comprehensive genetic analysis |
| Special Price | ZAR 6,700 | Save ZAR 2,650 |
Your investment includes: NGS genetic testing, genetic counselling session, comprehensive result analysis, and professional support throughout the process.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialised neurology-focused genetic testing
- Advanced Technology: State-of-the-art NGS methodology for maximum accuracy
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Professional Support: Genetic counselling included with every test
Take the First Step Toward Answers Today
Don’t let uncertainty about your infant’s health create unnecessary stress. Early detection through genetic testing can provide the clarity you need to make the best decisions for your child’s future.
Book your ARHGEF9 Epilepsy DNA Test now for just ZAR 6,700 and get:
- Comprehensive genetic analysis using NGS technology
- Professional genetic counselling session
- Clear, understandable results in 3-4 weeks
- Nationwide accessibility across South Africa
- Peace of mind and actionable health information
Contact Oracle Genomics today to schedule your test and take control of your child’s neurological health journey.
