Find Clarity About Hereditary Motor Neuron Disorders
When you notice progressive muscle weakness or have a family history of neurological conditions, the uncertainty can be overwhelming. Our DCTN1 Gene Neuronopathy Test provides the definitive answers you need to understand your genetic risk and plan for your health future with confidence.
Understanding Your DCTN1 Genetic Test
This advanced Next-Generation Sequencing (NGS) test examines the DCTN1 gene for mutations that cause Distal Hereditary Motor Neuropathy Type 7B. This condition affects the nerves controlling muscle movement, leading to progressive weakness that typically begins in the hands and feet. Our test provides comprehensive analysis with 99.9% accuracy, giving you reliable results you can trust for making important health decisions.
Who Should Consider This Genetic Test?
- Individuals experiencing progressive muscle weakness in hands or feet
- People with family members diagnosed with hereditary motor neuron disorders
- Those noticing difficulty with fine motor skills or walking coordination
- Individuals with unexplained muscle wasting or twitching
- Anyone concerned about passing neurological conditions to children
Early detection through genetic testing can help you and your healthcare team develop proactive management strategies.
Why This Test Matters for Your Neurological Health
Getting tested for DCTN1 gene mutations provides crucial benefits for your health journey:
- Early Intervention: Identify risks before significant symptoms develop
- Family Planning: Make informed decisions about having children
- Treatment Planning: Work with neurologists to create personalised care strategies
- Peace of Mind: Reduce uncertainty about your genetic health status
- Proactive Monitoring: Establish appropriate screening schedules
Understanding Your Test Results
Our genetic counselling team will carefully explain your results in clear, understandable terms. You’ll learn whether you carry DCTN1 gene mutations and what this means for your health. We provide comprehensive guidance on next steps, including specialist referrals and lifestyle recommendations. Remember, a positive result doesn’t mean symptoms will definitely develop, but it does empower you with knowledge for proactive health management.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| DCTN1 Gene NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
Includes genetic counselling session and comprehensive results interpretation
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Team: Specialist neurologists and certified genetic counsellors
- Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
- Quick Turnaround: Results in 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood drop
Take the First Step Toward Neurological Health Clarity
Don’t let uncertainty about hereditary conditions control your future. Our DCTN1 genetic test provides the answers you need to make empowered health decisions. With convenient testing locations nationwide and expert support throughout the process, you can approach your neurological health with confidence.
Early detection of hereditary motor neuron disorders can significantly impact treatment outcomes and quality of life. Take control of your neurological health today.
