Understanding Your Genetic Risk for Hereditary Spastic Paraplegia
When neurological symptoms run in your family, the uncertainty can be overwhelming. The HSPD1 Gene SPG13 NGS Genetic DNA Test provides the clarity you need to understand your genetic predisposition to hereditary spastic paraplegia. We understand the anxiety that comes with family health patterns, and we’re here to provide accurate, reliable answers with compassion and expertise.
What This Test Reveals About Your Health
The HSPD1 Gene SPG13 test uses advanced Next Generation Sequencing technology to detect specific mutations in the HSPD1 gene that are responsible for SPG13, a form of hereditary spastic paraplegia. This condition typically causes progressive stiffness and weakness in the legs, affecting mobility and quality of life. Our test doesn’t just provide results – it provides understanding and direction for your health journey.
Is This Test Right for You?
Consider the HSPD1 SPG13 genetic test if you experience:
- Progressive leg stiffness or weakness that runs in your family
- Difficulty with walking or balance that began in adulthood
- Family members diagnosed with hereditary spastic paraplegia
- Concerns about passing neurological conditions to children
- Unexplained muscle spasticity with family history
Early genetic insight can transform how you approach your neurological health and family planning decisions.
Why Early Detection Matters for Your Future
Knowing your genetic status empowers you to take control of your health journey. With definitive results, you can:
- Make informed family planning decisions with genetic counselling guidance
- Implement early intervention strategies to manage symptoms
- Reduce anxiety through clear understanding of your genetic risk
- Access appropriate neurological care and support services
- Participate in research and clinical trials if desired
Peace of mind comes from knowing, not wondering.
Understanding Your Genetic Results
Our comprehensive approach includes genetic counselling to help you interpret your results with confidence. You’ll receive:
- Clear, understandable explanation of your genetic findings
- Personalised discussion about what results mean for your health
- Guidance on next steps and available management options
- Family pedigree analysis to understand inheritance patterns
- Ongoing support and resources for your neurological health
We believe knowledge should empower, not overwhelm.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| HSPD1 SPG13 NGS Genetic Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
Your investment includes: Advanced NGS testing, genetic counselling session, comprehensive results interpretation, and ongoing support. Compared to potential lifelong healthcare costs of undiagnosed neurological conditions, this test represents significant value for your long-term health.
Why South Africans Trust Oracle Genomics
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Neurological Expertise: Tests supervised by specialist neurologists
- Advanced Technology: Next Generation Sequencing for 99.9% accuracy
- Genetic Counselling: Essential pre-test counselling included
- Quick Turnaround: Results within 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot card
Take Control of Your Genetic Health Today
Don’t let uncertainty about hereditary neurological conditions dictate your future. With our special pricing of ZAR 6,700, there’s never been a better time to gain clarity.
Limited Time Offer: Special pricing of ZAR 6,700 available for immediate bookings. Regular price ZAR 9,350. Take action today for peace of mind tomorrow.
