Finding Answers for Neurological Concerns: RNASEH2C Gene Testing
When your child shows unexplained neurological symptoms, the uncertainty can be overwhelming. Our RNASEH2C Gene Aicardi-Goutieres Syndrome Type 3 test provides the clarity you need to make informed healthcare decisions for your family. We understand the emotional journey you’re facing, and we’re here to support you with accurate, reliable genetic testing.
Understanding the RNASEH2C Gene Test
This specialised genetic test examines the RNASEH2C gene for mutations associated with Aicardi-Goutieres Syndrome Type 3, a rare neurological condition that typically appears in infancy. Using advanced Next-Generation Sequencing (NGS) technology, we provide comprehensive analysis with exceptional accuracy. The test requires only a simple blood sample or extracted DNA, making the process straightforward and minimally invasive for your child.
Who Should Consider This Test?
This test is particularly important for families where:
- Infants show unexplained neurological symptoms like developmental delays
- There’s a family history of similar neurological conditions
- Children experience seizures or movement disorders without clear cause
- Parents want to understand genetic risks for future family planning
- Medical professionals suspect Aicardi-Goutieres Syndrome based on clinical presentation
Why Early Detection Matters for Your Child’s Health
Early genetic diagnosis through our RNASEH2C test can significantly impact your child’s quality of life by:
- Enabling timely medical interventions and appropriate care planning
- Reducing diagnostic uncertainty and unnecessary medical procedures
- Providing clarity for family planning decisions
- Connecting you with specialised neurological care resources
- Offering peace of mind through definitive answers
Understanding Your Test Results
We know waiting for genetic test results can be anxiety-provoking. Our comprehensive approach includes:
- Clear, easy-to-understand result explanations
- Genetic counselling support to help interpret findings
- Guidance on next steps based on your results
- Connection to appropriate medical specialists if needed
- Ongoing support throughout your healthcare journey
Results are typically available within 3-4 weeks, and our team ensures you receive them with the care and attention they deserve.
Transparent Pricing – Investing in Your Family’s Health
| Service | Regular Price | Special Price |
|---|---|---|
| RNASEH2C Gene Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
This comprehensive package represents excellent value, considering the potential long-term healthcare savings from early, accurate diagnosis.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialised neurological genetic testing supervised by experienced professionals
- Advanced Technology: State-of-the-art NGS technology for maximum accuracy
- Comprehensive Support: Genetic counselling included with every test
- Proven Reliability: Trusted by healthcare professionals nationwide
Take the First Step Toward Clarity
Don’t let uncertainty about neurological symptoms continue to cause anxiety. Our RNASEH2C Gene Test provides the answers you need to move forward with confidence.
Limited Time Special: Book now to secure the special price of ZAR 6,700 before it returns to ZAR 9,350. Early detection could make all the difference for your child’s health journey.
“The peace of mind we gained from getting definitive answers was priceless. The Oracle Genomics team supported us every step of the way.” – Satisfied Parent
Nationwide Accessibility
We’re committed to making advanced genetic testing accessible to all South Africans. With collection points in major cities and remote testing options available, geographical location is no barrier to receiving the genetic clarity your family deserves.
