Find Clarity About Hereditary Ataxia with Our PRKCG Gene Test
When unexplained balance problems, coordination difficulties, or a family history of movement disorders leave you searching for answers, our PRKCG Gene Spinocerebellar Ataxia Type 14 test provides the clarity you need. This autosomal dominant condition can affect multiple generations, and understanding your genetic status empowers you to make informed decisions about your health and family planning.
Understanding the PRKCG Gene Test
The PRKCG gene test examines your DNA for mutations that cause Spinocerebellar Ataxia Type 14, a progressive neurological condition affecting coordination and balance. Using Next-Generation Sequencing (NGS) technology, we analyse the PRKCG gene with exceptional accuracy to identify the specific genetic changes responsible for this hereditary disorder.
This isn’t just a test – it’s a comprehensive health assessment that includes genetic counselling to help you understand how this condition may affect you and your family members.
Who Should Consider This Test?
This test is particularly important if you experience:
- Unexplained balance problems or frequent stumbling
- Progressive coordination difficulties affecting daily activities
- Family history of movement disorders or ataxia
- Planning for pregnancy with concerns about hereditary conditions
- Neurological symptoms without clear diagnosis
- Multiple family members with similar coordination issues
Early detection can significantly impact your quality of life and help you access appropriate management strategies sooner.
Why This Test Matters for Your Health
Getting tested provides crucial benefits that extend beyond diagnosis:
- Early Intervention: Identify ataxia before severe symptoms develop
- Family Planning: Make informed decisions about having children
- Peace of Mind: End the uncertainty about your genetic status
- Treatment Guidance: Work with neurologists on targeted management plans
- Family Awareness: Alert relatives who may be at risk
- Future Planning: Prepare for potential progression with confidence
Understanding Your Results
We make understanding your results straightforward and supportive:
- Positive Result: Indicates a PRKCG gene mutation. Our genetic counsellor will explain what this means for your health and provide guidance on next steps
- Negative Result: No mutation detected, providing reassurance about your genetic status
- Uncertain Variant: Rare genetic changes of unknown significance – we’ll explain what this means and recommend follow-up
Every result comes with professional genetic counselling to ensure you fully understand the implications and have a clear path forward.
Transparent Pricing & Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| PRKCG Gene Test with Genetic Counselling | ZAR 6,700 | ZAR 2,650 |
Your investment includes: Comprehensive NGS analysis, professional genetic counselling session, detailed results interpretation, and ongoing support from our neurological specialists.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Developed in consultation with leading neurologists
- Advanced Technology: Next-Generation Sequencing ensures 99.9% accuracy
- Complete Support: Genetic counselling included with every test
- Rapid Results: 3-4 week turnaround with clear explanations
- Confidential Service: Your privacy and data security are our priority
Take the First Step Toward Clarity
Don’t let uncertainty about hereditary ataxia control your future. Our PRKCG Gene Test provides the answers you need to take control of your neurological health.
What to expect: Simple blood sample or FTA card collection, comprehensive genetic counselling to understand your family history, and clear, supportive results within 3-4 weeks.
Limited Time Special: Save ZAR 2,650 on our comprehensive PRKCG Gene Test. Regular price ZAR 9,350 now only ZAR 6,700.
Book your test today and start your journey toward understanding your genetic health with confidence and clarity.
