Finding Answers for Neurological Development Concerns
When your child shows signs of developmental delays or neurological symptoms, the uncertainty can be overwhelming. The Aicardi-Goutieres Syndrome Test provides the clarity South African families need to understand complex neurological conditions and plan the right care pathway.
Understanding Aicardi-Goutieres Syndrome Testing
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects brain development and can cause progressive neurological problems. Our Next Generation Sequencing test examines seven critical genes – ADAR, IFIH1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and TREX1 – to identify mutations that may be responsible for neurological symptoms.
Using cutting-edge NGS technology combined with Sanger sequencing verification, we deliver comprehensive genetic analysis with exceptional accuracy. This approach ensures no important genetic variations are missed, giving you complete confidence in your results.
Who Should Consider This Test?
This test is particularly important for families noticing:
- Unexplained developmental delays in infancy or early childhood
- Progressive neurological symptoms without clear cause
- Family history of similar neurological conditions
- Abnormal brain imaging results suggesting genetic origins
- Multiple siblings affected by neurological disorders
If your child has been experiencing seizures, intellectual disability, or unusual movements that concern you, this test can provide the answers needed to guide appropriate medical care.
Why Early Detection Matters for Your Family’s Health
Early genetic diagnosis through AGS testing offers significant benefits:
- Accurate Diagnosis: Move from uncertainty to clear understanding of the condition
- Personalised Treatment: Guide healthcare providers toward appropriate interventions
- Family Planning: Understand inheritance patterns for future family decisions
- Reduced Medical Costs: Avoid unnecessary tests and treatments through precise diagnosis
- Peace of Mind: Replace anxiety with knowledge and a clear action plan
Many families find that receiving a definitive diagnosis, while challenging, provides relief from the uncertainty and enables them to focus on the most effective care strategies.
Understanding Your Test Results
We understand that waiting for genetic test results can be stressful. Our team provides clear, compassionate explanations of your findings:
- Positive Result: Indicates a genetic mutation associated with AGS – our genetic counsellors will explain what this means for care and management
- Negative Result: No AGS-related mutations detected – this helps rule out this specific condition
- Uncertain Variants: Sometimes we find genetic changes of unknown significance – we’ll explain what monitoring might be appropriate
Every result comes with guidance from our medical team to help you understand the implications and next steps. Remember, knowledge is power when it comes to managing complex neurological conditions.
Transparent Pricing – Exceptional Value
| Test Option | Price | Savings |
|---|---|---|
| Special Price | ZAR 7,800 | ZAR 900 savings |
| Regular Price | ZAR 8,700 | – |
Turnaround Time: Samples processed daily by 9 am | Results in 40 working days
Considering the cost of ongoing specialist consultations and unnecessary treatments, this one-time investment in accurate diagnosis represents significant long-term healthcare savings.
Why Trust Oracle Genomics?
We’ve built our reputation on accuracy, compassion, and accessibility across South Africa:
- Nationwide Coverage: Accessible testing from Johannesburg to Cape Town, Durban to Pretoria
- Expert Team: Specialised neurologists and geneticists overseeing every analysis
- Advanced Technology: State-of-the-art NGS with Sanger verification for maximum accuracy
- Patient-Focused: Clear communication and compassionate support throughout the process
- Proven Accuracy: 99.9% detection rate for targeted genetic variants
Our commitment to South African families means we understand the unique healthcare challenges and provide solutions that work within our local context.
Simple Sample Collection Process
Getting tested is straightforward:
- Sample Type: 10 mL (5 mL minimum) whole blood from 2 Lavender Top (EDTA) tubes
- Shipping: Refrigerated transport – DO NOT FREEZE
- Required Documentation: Duly filled Whole Exome Sequencing Consent Form (Form 37)
Our network of collection centres across major South African cities makes the process convenient and stress-free.
Take the First Step Toward Clarity Today
Don’t let uncertainty about neurological symptoms continue to cause anxiety. Early detection through genetic testing provides the foundation for appropriate care and management.
Book Your Test Now:
- Online booking available 24/7
- Phone consultations with our genetic specialists
- Multiple collection centre options nationwide
- Flexible payment options
Limited time special pricing of ZAR 7,800 – secure your test while this offer lasts. Every day of delay means another day without answers for your family’s health concerns.
Nationwide Accessibility
We serve patients across South Africa with convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria, and surrounding areas. Wherever you are, we’re here to help.
