Find Clarity About Hereditary Spastic Paraplegia with KIF5A Genetic Testing
When neurological symptoms run in your family, the uncertainty can be overwhelming. You deserve definitive answers about your genetic risk for SPG10 – a form of hereditary spastic paraplegia that affects mobility and quality of life. Our KIF5A Gene SPG10 NGS Genetic DNA Test provides the medical certainty you need to make informed decisions about your health journey.
Understanding Your KIF5A SPG10 Genetic Test
The KIF5A gene plays a crucial role in nerve cell function, and mutations in this gene can lead to SPG10 – a progressive neurological condition affecting muscle control and movement. Our advanced Next Generation Sequencing (NGS) technology examines your DNA with exceptional precision, identifying even the smallest genetic variations that could indicate SPG10 risk.
This isn’t just another test – it’s a comprehensive genetic analysis that provides life-changing information about your neurological health inheritance patterns.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Progressive leg stiffness and muscle weakness
- Difficulty walking that worsens over time
- Family history of similar neurological symptoms
- Unexplained balance or coordination issues
- Early-onset mobility challenges in relatives
- Concerns about passing genetic conditions to children
Many South African families live with undiagnosed hereditary conditions for generations. This test can break that cycle of uncertainty.
Why Early Detection Matters for Your Health
Knowing your genetic status empowers you to:
- Make informed family planning decisions
- Access appropriate medical care and interventions
- Connect with specialist neurologists who understand SPG10
- Participate in monitoring programs for early symptom management
- Reduce anxiety through definitive genetic information
- Plan for your future health needs with confidence
Early genetic insight can significantly improve quality of life through proactive management strategies.
Understanding Your Test Results
Your results will be clearly explained by our genetic counselling team, who will help you understand:
- Whether a KIF5A gene mutation was detected
- What the findings mean for your health
- Recommended next steps and specialist referrals
- Implications for family members
- Available management and support options
We believe knowledge should bring peace, not panic. Our team ensures you leave with clarity and a practical action plan.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| KIF5A SPG10 NGS Genetic Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
What’s Included: Comprehensive genetic analysis, genetic counselling session, detailed results interpretation, and professional report for your healthcare provider.
Turnaround Time: 3-4 weeks from sample receipt
Sample Type: Blood, extracted DNA, or one drop blood on FTA card
Why Trust Oracle Genomics?
- Nationwide Coverage: Testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS technology for 99.9% accuracy
- Patient Privacy: Strict confidentiality and ethical standards maintained
- Genetic Counselling: Pre-test counselling to create your family pedigree chart
- South African Focus: Understanding local healthcare needs and family dynamics
Take Control of Your Genetic Health Today
Don’t let uncertainty about hereditary spastic paraplegia control your future. With our special pricing of ZAR 6,700, there’s never been a better time to gain the genetic clarity you deserve.
Limited Time Offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) won’t last forever. Secure your genetic health assessment while savings are available.
Every day you wait is another day without answers. Take the first step toward genetic certainty and peace of mind. Our team is ready to support you through this important health journey.
