Find Clarity About Hereditary Movement Disorders
When coordination problems, balance issues, or unexplained neurological symptoms affect your family, the uncertainty can be overwhelming. Our PLEKHG4 Gene Spinocerebellar Ataxia Type 4 test provides the definitive answers you need to understand your genetic risk and plan for the future with confidence.
Understanding Your PLEKHG4 Ataxia Test
This advanced genetic test specifically examines the PLEKHG4 gene for mutations that cause Spinocerebellar Ataxia Type 4 – an inherited neurological condition that affects coordination, balance, and movement control. Using Next-Generation Sequencing (NGS) technology, we analyse your DNA with exceptional precision to identify even the smallest genetic variations that could indicate this condition.
What makes this test particularly important is its autosomal dominant nature – meaning if one parent carries the gene mutation, there’s a 50% chance of passing it to each child. Early detection through our testing can help you and your healthcare team develop proactive management strategies.
Who Should Consider This Test?
This test is especially relevant if you or your family members experience:
- Progressive coordination difficulties or unsteady gait
- Family history of movement disorders or ataxia
- Unexplained balance problems that seem to run in the family
- Speech difficulties or swallowing problems with genetic patterns
- Planning for pregnancy with known family history of neurological conditions
Many South African families with European ancestry may have increased risk factors, making this test particularly valuable for comprehensive family health planning.
Why Early Detection Matters for Your Health
Knowing your genetic status provides powerful advantages:
- Peace of Mind: Eliminate uncertainty about your genetic risk factors
- Proactive Management: Work with neurologists to monitor and manage potential symptoms early
- Family Planning: Make informed decisions about starting a family
- Treatment Planning: Coordinate with healthcare providers for appropriate interventions
- Reduced Anxiety: Replace fear of the unknown with concrete information and action plans
Understanding Your Results with Compassion
We understand that genetic testing can feel overwhelming. That’s why every test includes professional genetic counselling to help you interpret your results in the context of your family history. Our specialists will explain:
- What your specific genetic findings mean for your health
- How to discuss results with family members appropriately
- Next steps for monitoring and management if needed
- Resources and support available throughout South Africa
Your results will be clearly explained, with ample time for questions and thorough understanding.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| PLEKHG4 Ataxia Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | Included at no extra cost | ||
| Family Pedigree Analysis | Comprehensive assessment included | ||
Consider the long-term value: Early detection can save significantly on future healthcare costs and provide priceless peace of mind.
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS sequencing for 99.9% accuracy
- Rapid Turnaround: Results typically within 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood drop
- Professional Support: Comprehensive genetic counselling included with every test
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about hereditary conditions control your family’s future. With our special pricing of ZAR 6,700, now is the perfect time to gain the clarity you deserve.
Limited Time Offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) won’t last forever. Secure your family’s genetic health today.
“The peace of mind from knowing our genetic status has been invaluable for our family’s future planning.” – Recent Patient, Cape Town
