Find Clarity About Hereditary Spastic Paraplegia in Your Family
When you notice mobility challenges or neurological symptoms running in your family, the uncertainty can be overwhelming. The ERLIN2 Gene SPG18 NGS Genetic DNA Test provides the answers you need to understand your genetic risk and make informed decisions about your family’s health future.
Understanding Your ERLIN2 SPG18 Genetic Test
This advanced Next Generation Sequencing (NGS) test specifically examines the ERLIN2 gene for mutations that cause SPG18, a form of hereditary spastic paraplegia. Unlike basic genetic screenings, our comprehensive analysis provides detailed insights into your genetic makeup, helping you understand whether you carry mutations that could affect your mobility or be passed to future generations.
The test is performed using state-of-the-art NGS technology, ensuring the highest accuracy and reliability in genetic analysis. We process either blood samples, extracted DNA, or a simple blood drop on an FTA card, making the testing process convenient and accessible.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Progressive stiffness and weakness in the legs
- Difficulty with walking that worsens over time
- Family history of similar mobility challenges
- Concerns about passing neurological conditions to children
- Unexplained spasticity or muscle tightness
- Early signs of gait abnormalities
If you’re planning a family and have concerns about hereditary conditions, this test provides crucial information for making informed reproductive decisions.
Why This Test Matters for Your Health Journey
Early detection of ERLIN2 gene mutations can significantly impact your quality of life and family planning decisions. By understanding your genetic status, you can:
- Access appropriate medical management and interventions early
- Make informed family planning decisions with genetic counselling support
- Reduce anxiety through clarity and certainty about your genetic status
- Participate in proactive healthcare rather than reactive treatment
- Connect with appropriate specialists and support networks
Many patients experience tremendous relief simply from having answers, allowing them to move forward with confidence in their healthcare decisions.
Understanding Your Test Results
Our genetic counsellors will guide you through your results with compassion and expertise. You’ll receive a comprehensive report that clearly explains:
- Whether ERLIN2 gene mutations were detected
- The specific implications for your health and family members
- Recommended next steps and specialist consultations
- Options for family testing and genetic counselling
- Resources and support networks available in South Africa
Remember: A positive result doesn’t necessarily mean you’ll develop symptoms, and our team will help you understand what your specific results mean for your health journey.
Transparent Pricing & Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| ERLIN2 SPG18 NGS Genetic Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Consultation | Included | |
Consider this investment in your health: Early detection can save significantly on future medical costs and provide peace of mind that’s truly priceless.
Why Trust Oracle Genomics?
We understand that genetic testing requires absolute confidence in your healthcare provider. That’s why we offer:
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Neurological Expertise: Tests reviewed by specialist neurologists familiar with hereditary spastic paraplegia
- Genetic Counselling: Comprehensive pre- and post-test counselling included in your package
- Proven Accuracy: State-of-the-art NGS technology ensuring reliable results
- Patient-Centred Care: Empathetic support throughout your testing journey
- Fast Turnaround: Results typically within 3-4 weeks
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about hereditary conditions control your family’s future. Our genetic counsellors are ready to help you understand your risk and make empowered healthcare decisions.
Book your genetic counselling session today and take control of your health journey.
Available testing options:
- Blood sample collection at our nationwide centres
- Extracted DNA analysis for patients with existing samples
- Convenient FTA card blood drop method
Contact us now to schedule your appointment and begin your journey to genetic clarity.
