Understanding Hereditary Spastic Paraplegia: Your Path to Clarity
When walking becomes increasingly difficult or muscle stiffness affects your daily life, the uncertainty can be overwhelming. Many South Africans face these challenges without understanding the underlying cause, particularly when similar symptoms appear across generations in their family. Our PNPLA6 Gene SPG39 NGS Genetic DNA Test is designed to provide the answers you deserve, using cutting-edge technology to identify hereditary spastic paraplegia with exceptional accuracy.
What This Test Detects
The PNPLA6 gene test specifically identifies mutations associated with SPG39, a form of hereditary spastic paraplegia that affects the nervous system. This condition typically causes progressive stiffness and weakness in the legs, making walking increasingly challenging over time. Our advanced Next-Generation Sequencing (NGS) technology examines your DNA with precision, looking for the specific genetic variations that cause this inherited neurological condition.
Who Should Consider This Test
This test is particularly important if you or your family members experience:
- Progressive difficulty walking or unusual gait
- Muscle stiffness and spasms in the legs
- Family history of similar neurological symptoms
- Unexplained balance problems or frequent falls
- Early-onset walking difficulties in childhood or young adulthood
Why Early Detection Matters for Your Health
Understanding your genetic status provides more than just answers – it offers empowerment. With a confirmed diagnosis, you can:
- Access appropriate treatments and management strategies
- Make informed family planning decisions
- Connect with specialist neurologists who understand your condition
- Participate in relevant support communities and research
- Plan for future healthcare needs with confidence
Understanding Your Results: Clear Guidance Every Step
We know that waiting for genetic test results can be anxiety-provoking. That’s why our process includes comprehensive genetic counselling both before and after testing. Your results will be clearly explained by our specialists, who will help you understand what they mean for your health and your family. Whether the test identifies a mutation or provides reassuring negative results, you’ll receive the support and guidance needed to move forward with confidence.
Transparent Pricing & Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| PNPLA6 SPG39 Genetic Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | Included at no extra cost | |
| Results Turnaround | 3-4 weeks | |
Nationwide Accessibility & Trust
Oracle Genomics brings expert genetic testing to communities across South Africa. With collection facilities in Johannesburg, Cape Town, Durban, Pretoria and other major centres, accessing this important health information has never been more convenient. Our team of neurologists and genetic specialists ensures that every test is conducted with the highest standards of accuracy and care.
Take the First Step Toward Clarity
Don’t let uncertainty about your neurological health continue to cause worry. Our PNPLA6 SPG39 genetic test provides the definitive answers you need to take control of your health journey. With our special pricing of ZAR 6,700 and comprehensive support services, there’s never been a better time to seek the clarity you deserve.
Book your test today and begin your journey to understanding. Contact us to schedule your genetic counselling session and testing appointment at a location convenient for you.
