Find Clarity About Hereditary Motor Neuron Conditions
When movement difficulties run in your family, the uncertainty can be overwhelming. Our HSPB8 Gene Neuronopathy Test provides the answers you need to understand your genetic risk and take control of your neurological health journey.
Understanding Your HSPB8 Gene Test
This advanced genetic screening examines the HSPB8 gene, which plays a crucial role in maintaining healthy motor neurons. When mutations occur in this gene, it can lead to distal hereditary motor neuronopathy type 2A – a condition affecting the nerves that control muscle movement in your hands and feet.
Using Next Generation Sequencing (NGS) technology, we provide the most accurate analysis available, giving you reliable information about your genetic makeup and potential health risks.
Who Should Consider This Genetic Test?
- Individuals with family history of movement disorders or muscle weakness
- People experiencing unexplained hand or foot weakness
- Those with relatives diagnosed with hereditary motor neuron diseases
- Couples planning pregnancy with neurological conditions in family history
- Individuals seeking proactive health screening for inherited conditions
If you’ve noticed progressive weakness in your hands or feet, or have concerns about inherited neurological conditions, this test can provide the clarity you deserve.
Why Early Detection Matters for Your Health
Knowing your genetic status empowers you to make informed health decisions. Early detection of HSPB8 gene mutations allows for:
- Proactive management strategies
- Better understanding of symptom progression
- Informed family planning decisions
- Access to appropriate specialist care
- Peace of mind through genetic counselling
Many patients find tremendous relief in having definitive answers, even when results indicate increased risk.
Understanding Your Test Results
Our comprehensive genetic counselling ensures you fully understand your results and their implications. We’ll help you:
- Interpret what your genetic findings mean for your health
- Create a family pedigree chart to understand inheritance patterns
- Develop a personalised health management plan
- Connect with neurological specialists if needed
- Understand options for family members
Remember: A positive result doesn’t mean symptoms will definitely develop, and our team will guide you through all possible outcomes.
Transparent Pricing – Your Health Investment
| Service | Regular Price | Special Price |
|---|---|---|
| HSPB8 Gene Test with Genetic Counselling | ZAR 6,700 | |
| Turnaround Time | 3-4 Weeks | |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | |
Consider this: Early detection could save you from years of uncertainty and potentially costly late-stage treatments.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: Using cutting-edge NGS sequencing for maximum accuracy
- Patient-Centred Care: Comprehensive genetic counselling included with every test
- Proven Reliability: Trusted by healthcare professionals nationwide
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about hereditary conditions control your life. Our team is ready to provide the answers and support you need.
Limited Time Special: Save ZAR 2,650 on your HSPB8 gene test. Book now to secure this special pricing and take control of your genetic health journey.
