Find Clarity About Hereditary Spastic Paraplegia
When unexplained muscle stiffness, walking difficulties, or neurological symptoms affect multiple family members, the uncertainty can be overwhelming. You deserve answers about whether hereditary spastic paraplegia (SPG6) runs in your family. Our NIPA1 Gene SPG6 NGS Genetic DNA Test provides the clarity and peace of mind you need to make informed health decisions.
Understanding Your NIPA1 SPG6 Genetic Test
This advanced genetic test specifically examines the NIPA1 gene, which is responsible for SPG6 – a form of hereditary spastic paraplegia. Using Next Generation Sequencing (NGS) technology, we analyse your DNA with exceptional accuracy to identify mutations that could cause neurological symptoms. The test is straightforward – requiring only a blood sample or simple DNA collection – and provides results you can trust.
Who Should Consider This Test?
This test is particularly important if you or family members experience:
- Progressive muscle stiffness and weakness in the legs
- Difficulty walking that worsens over time
- Family history of similar neurological symptoms
- Unexplained balance problems or frequent falls
- Muscle spasms or increased reflexes
- Concerns about passing neurological conditions to children
If multiple relatives show similar symptoms, genetic testing can provide crucial answers about inheritance patterns.
Why Early Detection Matters for Your Health
Getting answers about SPG6 provides significant benefits:
- Peace of Mind: End the uncertainty about your family’s neurological health
- Early Intervention: Begin appropriate management strategies sooner
- Family Planning: Make informed decisions about having children
- Treatment Guidance: Work with neurologists on targeted care plans
- Prevent Complications: Address symptoms before they significantly impact daily life
Understanding Your Results with Confidence
We understand that waiting for genetic results can be anxiety-provoking. That’s why we provide:
- Clear Explanations: Results are explained in understandable language
- Genetic Counselling: Professional guidance to interpret what your results mean
- Family Context: Help understanding how results affect your relatives
- Next Steps: Practical recommendations based on your specific situation
- Ongoing Support: Access to resources and specialists as needed
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| NIPA1 Gene SPG6 NGS Genetic DNA Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Explanation | Included | |
Considering the lifelong impact of neurological conditions, this investment in your health provides invaluable clarity and potential savings on future medical costs.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Neurological Focus: Specialised in neurological genetic conditions
- Advanced Technology: Using cutting-edge NGS sequencing for maximum accuracy
- Professional Genetic Counselling: Every test includes expert guidance
- Proven Track Record: Trusted by neurologists and patients nationwide
- Rapid Turnaround: Results typically within 3-4 weeks
Take the First Step Toward Clarity
Don’t let uncertainty about hereditary neurological conditions control your family’s future. Our comprehensive approach includes genetic counselling to create your family health history, ensuring you get the most accurate interpretation of your results.
Limited Time Offer: Save ZAR 2,650 on your genetic testing
Convenient Locations: Testing available nationwide
Expert Support: Genetic counselling included with every test
