Understanding Aicardi-Goutieres Syndrome: Your Path to Clarity
When your child shows unexplained neurological symptoms, the uncertainty can be overwhelming. Aicardi-Goutieres syndrome is a rare genetic condition that affects brain development, and getting clear answers is crucial for your family’s peace of mind. Our RNASEH2B gene test provides the definitive diagnosis you need to move forward with confidence.
What This Test Detects
This advanced genetic test specifically examines the RNASEH2B gene for mutations that cause Aicardi-Goutieres syndrome type 2. Using Next-Generation Sequencing (NGS) technology, we can identify even the smallest genetic variations with exceptional accuracy. This isn’t just a test – it’s a comprehensive genetic analysis that gives you clear, actionable information about your child’s neurological health.
Who Should Consider This Test
This test is particularly important if your child shows:
- Unexplained developmental delays or regression
- Microcephaly (small head size)
- Seizures or abnormal movements
- Skin lesions or chilblains
- Family history of similar neurological conditions
- Unexplained irritability or feeding difficulties in infancy
Why Early Detection Matters for Your Family
Getting an accurate diagnosis early can significantly impact your child’s quality of life. With clear genetic information, you can:
- Access appropriate medical care and interventions sooner
- Make informed decisions about family planning
- Connect with specialist healthcare providers
- Reduce the stress of uncertainty and multiple doctor visits
- Develop a targeted care plan for your child’s specific needs
Understanding Your Results with Compassion
We know that waiting for genetic test results can be anxiety-provoking. That’s why every test includes professional genetic counselling to help you understand your results in clear, compassionate terms. Our genetic counsellors will:
- Explain your results in simple, understandable language
- Create a family pedigree chart to visualize inheritance patterns
- Discuss what the results mean for your child’s health management
- Provide guidance on next steps and available support resources
- Address any questions or concerns you may have
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price |
|---|---|---|
| RNASEH2B Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | INCLUDED | |
| Family Pedigree Analysis | INCLUDED | |
| Results Interpretation | INCLUDED | |
Why Trust Oracle Genomics?
As South Africa’s leading genetic testing provider, we combine medical excellence with compassionate care:
- 99.9% Accuracy: Our NGS technology ensures reliable results you can trust
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Team: Working with qualified neurologists and genetic specialists
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Clear Timeline: Results delivered within 3-4 weeks
Take the First Step Toward Clarity
Don’t let uncertainty about your child’s neurological health continue to cause stress. Our RNASEH2B gene test provides the answers you need to make informed decisions about your family’s future.
Book Your Test Today: Call 0861 123 456 or visit our website to schedule your genetic counselling session and testing. Early detection can make all the difference in managing Aicardi-Goutieres syndrome effectively.
Oracle Genomics – Providing South African families with accurate genetic testing and compassionate care since 2010.
