Find Clarity About Hereditary Spastic Paraplegia with Our FA2H Gene SPG35 DNA Test
Living with unexplained walking difficulties or watching a loved one struggle with progressive mobility issues can be overwhelming. The uncertainty about whether these symptoms are related to hereditary spastic paraplegia can create significant anxiety. Our FA2H Gene SPG35 NGS Genetic DNA Test provides the definitive answers you need to understand your neurological health and plan for the future with confidence.
Understanding Your FA2H Gene SPG35 Test
This advanced genetic test specifically examines the FA2H gene using Next-Generation Sequencing (NGS) technology, the gold standard in genetic analysis. The FA2H gene plays a crucial role in maintaining healthy nerve function, and mutations in this gene are directly linked to hereditary spastic paraplegia type 35 (SPG35). Our test provides comprehensive analysis of this gene, giving you clear, reliable results to guide your healthcare journey.
Who Should Consider This Genetic Test?
This test is particularly important if you experience:
- Progressive difficulty walking or unusual gait patterns
- Muscle stiffness or spasticity in your legs
- Family history of similar neurological symptoms
- Unexplained balance problems or frequent falls
- Concerns about passing genetic conditions to children
- Early signs of mobility issues without clear diagnosis
If you recognize these symptoms in yourself or family members, our test can provide the clarity needed for proper management and treatment planning.
Why Early Detection Matters for Your Health
Getting answers about SPG35 through genetic testing offers significant benefits:
- Peace of Mind: Eliminate uncertainty about your symptoms and genetic risks
- Early Intervention: Begin appropriate management strategies sooner
- Family Planning: Make informed decisions about having children
- Treatment Guidance: Work with neurologists to develop targeted care plans
- Proactive Health Management: Monitor and manage symptoms effectively
Understanding Your Test Results
We make understanding your results straightforward and reassuring. Our comprehensive genetic counselling session before testing ensures you’re fully prepared, and our clear result reporting explains exactly what your findings mean for your health. Whether your results show a mutation in the FA2H gene or provide reassuring negative results, you’ll have the information needed to move forward with confidence.
Transparent Pricing & Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| FA2H Gene SPG35 NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Includes genetic counselling session and comprehensive result analysis | |||
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why Trust Oracle Genomics?
We understand that genetic testing requires absolute confidence in accuracy and professionalism. That’s why we provide:
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Expert Genetic Counselling: Professional guidance throughout your testing journey
- Advanced NGS Technology: Gold-standard genetic analysis for reliable results
- Neurology Specialization: Tests developed and interpreted by neurological experts
- Patient-Centered Care: Empathetic support from initial consultation to result delivery
Take the First Step Toward Clarity Today
Don’t let uncertainty about hereditary spastic paraplegia control your life. Our FA2H Gene SPG35 test provides the answers you need to take control of your neurological health. With our special pricing of ZAR 6,700 and comprehensive support, there’s never been a better time to get the clarity you deserve.
Book your genetic counselling session now and begin your journey to understanding.
Available nationwide across South Africa. Fast, accurate results you can trust.
