Find Clarity for Hereditary Movement Disorders
When unexplained movements, tremors, or coordination challenges affect your daily life, the uncertainty can be overwhelming. You deserve answers, and our NKX2-1 Gene Chorea Hereditary Benign NGS Genetic DNA Test provides the clarity you need to move forward with confidence.
Understanding Your NKX2-1 Gene Chorea Test
This specialised genetic test examines the NKX2-1 gene, which plays a crucial role in brain development and movement control. Using advanced Next Generation Sequencing (NGS) technology, we can identify specific genetic variations that may cause hereditary benign chorea – a condition characterised by involuntary, dance-like movements that typically begin in childhood.
Our comprehensive approach includes genetic counselling to help map your family history, ensuring we provide the most accurate assessment of your genetic risk factors.
Who Should Consider This Important Test?
This test is particularly important if you or your family members experience:
- Involuntary, jerky movements that began in childhood
- Family history of similar movement disorders
- Unexplained coordination difficulties
- Concerns about passing genetic conditions to children
- Multiple family members with neurological symptoms
Early detection can provide crucial information for managing symptoms and making informed healthcare decisions.
Why This Test Matters for Your Health Journey
Getting clear answers about hereditary benign chorea can transform your healthcare experience by:
- Providing definitive diagnosis and ending diagnostic uncertainty
- Enabling targeted treatment and management strategies
- Informing family planning decisions with genetic counselling
- Reducing anxiety through clear understanding of your condition
- Connecting you with appropriate neurological care and support
Understanding Your Results with Confidence
Our genetic counsellors will walk you through your results in clear, understandable language. Whether your test identifies a genetic variation or provides reassuring negative results, you’ll receive:
- Comprehensive explanation of findings
- Personalised recommendations for next steps
- Connection to neurological specialists if needed
- Ongoing support for your healthcare journey
Remember: A positive result doesn’t define your future – it empowers you to take control of your health.
Transparent Pricing for Peace of Mind
| Service | Regular Price | Special Price |
|---|---|---|
| NKX2-1 Gene Chorea Test | ZAR 9,350 | ZAR 6,700 |
| Includes Genetic Counselling | ✓ Included | |
| Turnaround Time | 3-4 Weeks | |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | |
This investment in your health can save years of uncertainty and provide direction for effective management.
Why South Africans Trust Oracle Genomics
We understand that genetic testing requires absolute confidence in accuracy and professionalism. That’s why we provide:
- Nationwide Coverage – Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Advanced NGS Technology – State-of-the-art genetic sequencing for maximum accuracy
- Expert Genetic Counselling – Professional guidance throughout your testing journey
- Neurology Specialisation – Tests developed and interpreted by neurological experts
- Patient-First Approach – Empathetic support every step of the way
Take the First Step Toward Clarity Today
Don’t let uncertainty about hereditary movement disorders control your life. Our team is ready to help you get the answers you deserve.
Book Your Test Now: Call us directly or visit our website to schedule your genetic counselling session and testing.
Early detection leads to better management and peace of mind. Your journey to understanding starts here.
