Find Clarity About Joubert Syndrome in Your Family
When neurological concerns affect your loved ones, the uncertainty can be overwhelming. Our TCTN2 Gene Joubert Syndrome Type 24 NGS Genetic DNA Test provides the answers you need to make informed decisions about your family’s health journey. Using cutting-edge genetic technology, we help South African families understand their genetic risks with compassion and precision.
Understanding the TCTN2 Joubert Syndrome Test
This specialised genetic test examines the TCTN2 gene using Next Generation Sequencing (NGS) technology – the gold standard in genetic analysis. The TCTN2 gene plays a crucial role in brain development, and mutations in this gene are associated with Joubert syndrome type 24, a rare neurological condition affecting the cerebellum. Our test provides comprehensive analysis to detect these specific genetic variations with exceptional accuracy.
Who Should Consider This Test?
This test is particularly important if you or your family members experience:
- Abnormal eye movements or vision problems
- Delayed motor development in infants and children
- Breathing pattern abnormalities
- Intellectual disability or learning challenges
- Family history of Joubert syndrome or related neurological conditions
- Unexplained developmental delays in childhood
Many South African families find peace of mind through early detection, allowing for better planning and management of care.
Why This Test Matters for Your Family’s Health
Early genetic testing for Joubert syndrome provides numerous benefits:
- Early Intervention: Identify risks before symptoms become severe
- Family Planning: Make informed decisions about future pregnancies
- Personalised Care: Develop targeted treatment and management plans
- Peace of Mind: Reduce uncertainty about genetic risks
- Medical Guidance: Work with specialists to create the best care approach
Understanding Your Test Results
We understand that waiting for genetic results can be stressful. Our process is designed to provide clarity and support:
- Comprehensive Analysis: Detailed report of TCTN2 gene variations
- Genetic Counselling: Professional interpretation of your results
- Clear Explanations: Easy-to-understand findings and implications
- Next Steps Guidance: Recommendations for follow-up care if needed
- Family Implications: Understanding what results mean for relatives
Our genetic counsellors are available to help you understand your results and discuss appropriate next steps.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| TCTN2 Joubert Syndrome NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
Your investment includes: Comprehensive genetic analysis, professional genetic counselling session, detailed results report, and ongoing support. Considering the lifelong impact of early detection, this test represents exceptional value for your family’s health.
Why Trust Oracle Genomics?
We’re committed to providing South African families with reliable genetic testing services:
- Nationwide Coverage: Accessible testing across South Africa, including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Collaboration with neurologists and genetic specialists
- Advanced Technology: NGS technology for maximum accuracy
- Quick Turnaround: Results within 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or blood spot on FTA card
- Professional Support: Genetic counselling included with every test
Take the First Step Toward Clarity
Don’t let uncertainty about Joubert syndrome create unnecessary stress for your family. With our special pricing of ZAR 6,700, now is the perfect time to gain the genetic insights you need.
Limited Time Offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) won’t last forever. Secure your family’s health future while saving ZAR 2,650.
“The peace of mind we gained from understanding our genetic risks was priceless. The professional guidance made all the difference.” – Satisfied Oracle Genomics Patient
