Understanding Your Genetic Health Journey
When you notice unusual skin changes or have a family history of Neurofibromatosis-like symptoms, it’s natural to feel concerned and uncertain. The SPRED1 Gene Neurofibromatosis Type 1-Like Syndrome test is designed to provide the answers you need with compassion and scientific accuracy. This condition, while rare, can significantly impact quality of life, and early detection through genetic testing offers the opportunity for proactive health management.
What Does This Test Detect?
Our advanced Next-Generation Sequencing (NGS) technology examines the SPRED1 gene for mutations that cause Legius syndrome, a condition that closely resembles Neurofibromatosis type 1. Unlike traditional methods, NGS provides comprehensive analysis of the entire gene, ensuring no mutation goes undetected. This precision testing helps distinguish between different genetic conditions with similar symptoms, giving you and your healthcare provider the clarity needed for accurate diagnosis and appropriate care planning.
Who Should Consider This Test?
This test is particularly important if you or your family members experience:
- Multiple café-au-lait spots (light brown skin patches)
- Axillary or inguinal freckling
- Family history of Neurofibromatosis-like symptoms
- Unexplained learning difficulties or developmental delays
- Macrocephaly (larger than average head size)
- Lipomas or other benign growths
If you’re planning a family and have concerns about genetic inheritance, this test provides valuable information for making informed reproductive decisions.
Why Early Detection Matters for Your Health
Identifying SPRED1 gene mutations early offers significant health advantages:
- Peace of Mind: Eliminate uncertainty about your genetic status
- Proactive Management: Work with specialists to monitor and manage potential symptoms
- Family Planning: Make informed decisions about genetic inheritance risks
- Accurate Diagnosis: Ensure you receive appropriate medical care and avoid unnecessary treatments
- Reduced Anxiety: Replace worry with knowledge and a clear health plan
Understanding Your Test Results
Our comprehensive genetic counselling ensures you fully understand your results and their implications. We provide:
- Clear explanation of positive, negative, or variant of uncertain significance results
- Guidance on what your results mean for your health and family
- Recommendations for follow-up care and specialist consultations
- Support in discussing results with family members when appropriate
- Ongoing access to genetic counselling for any additional questions
Transparent Pricing and Value
| Service | Regular Price | Special Price |
|---|---|---|
| SPRED1 Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Consider this investment in your health: early detection can prevent years of uncertainty and potentially reduce future healthcare costs through targeted, appropriate care.
Why Trust Oracle Genomics?
We understand that genetic testing involves both scientific precision and human compassion. Our commitment includes:
- Nationwide Coverage: Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Collaboration with leading oncologists and genetic specialists
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Patient-Centred Care: Empathetic support throughout your testing journey
- Rapid Turnaround: Results typically within 3-4 weeks
Take the First Step Toward Clarity
Don’t let uncertainty about your genetic health create unnecessary worry. Our simple testing process begins with a genetic counselling session to understand your family history, followed by a convenient blood sample collection. With locations across South Africa and comprehensive support throughout the process, getting answers has never been more accessible.
Book your SPRED1 gene test today at the special price of ZAR 6,700 and take control of your genetic health journey. Early detection provides the foundation for informed health decisions and peace of mind for you and your family.
