Understanding Aicardi-Goutieres Syndrome Type 4: Finding Answers for Your Family
When your child shows neurological symptoms, the uncertainty can be overwhelming. Aicardi-Goutieres syndrome type 4 is a rare genetic disorder that affects brain development, often presenting in infancy with symptoms that may resemble congenital infections. Our RNASEH2A gene test provides the clarity you need to understand your child’s condition and make informed decisions about their care.
What This Test Detects
This advanced genetic test specifically examines the RNASEH2A gene for mutations associated with Aicardi-Goutieres syndrome type 4. Using Next-Generation Sequencing (NGS) technology, we analyse your DNA with exceptional accuracy to identify any genetic variations that could be causing neurological symptoms. The test provides definitive information about whether your child carries the genetic markers for this condition.
Who Should Consider This Test
This test is particularly important for families where:
- Infants show unexplained neurological symptoms like seizures or developmental delays
- There’s a family history of similar neurological conditions
- Children present with symptoms resembling congenital infections without confirmed diagnosis
- Parents are planning future pregnancies and want to understand genetic risks
- Current symptoms suggest Aicardi-Goutieres syndrome but require genetic confirmation
Why Early Genetic Testing Matters
Getting a definitive diagnosis through genetic testing can transform your family’s journey. Early detection allows for:
- Targeted treatment approaches and better symptom management
- Informed family planning decisions
- Access to appropriate support services and resources
- Reduced diagnostic uncertainty and emotional stress
- Connection with specialist care and support networks
Understanding Your Results
Our comprehensive approach includes genetic counselling to help you understand your results. We’ll explain what the findings mean for your child’s health and your family’s future. Whether the results confirm Aicardi-Goutieres syndrome or rule it out, you’ll have the information needed to move forward with confidence and appropriate medical care.
Pricing and Value
| Service | Regular Price | Special Price |
|---|---|---|
| RNASEH2A Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
Considering the potential impact on your child’s lifelong health and wellbeing, this investment in genetic clarity provides invaluable peace of mind and direction for future care.
Nationwide Accessibility
We provide comprehensive genetic testing services across South Africa, with convenient locations in Johannesburg, Cape Town, Durban, Pretoria and nationwide. Our network ensures you can access expert genetic testing and counselling regardless of your location.
Take the Next Step Towards Clarity
Don’t let uncertainty about your child’s neurological symptoms continue to cause anxiety. Our RNASEH2A gene test provides the answers you need to make informed decisions about your family’s health future. With results typically available within 3-4 weeks and comprehensive genetic counselling included, you’ll have the support and information needed to move forward with confidence.
Book your genetic counselling session today and take the first step toward understanding your family’s genetic health. Our team of specialists is ready to provide the compassionate, professional care your family deserves.
