Understanding Joubert Syndrome Type 16: Your Path to Genetic Clarity
When neurological concerns affect your family, the uncertainty can be overwhelming. Our TMEM138 Gene Joubert Syndrome Type 16 test provides the definitive answers you need to move forward with confidence. For South African families facing developmental delays or neurological symptoms, this test offers more than just results—it offers peace of mind and a clear path forward.
What This Test Detects
The TMEM138 gene test specifically identifies mutations associated with Joubert Syndrome Type 16, a rare neurological disorder that affects brain development. Using Next-Generation Sequencing (NGS) technology, we examine the TMEM138 gene with exceptional accuracy, providing you with reliable information about your genetic status.
This isn’t just a test—it’s a comprehensive health assessment that includes genetic counselling to help you understand your results in the context of your family’s health history.
Who Should Consider This Test?
This test is particularly important if you or your child experience:
- Developmental delays in motor skills or speech
- Abnormal eye movements or vision problems
- Breathing pattern abnormalities
- Poor muscle coordination or balance issues
- Family history of Joubert Syndrome or related neurological conditions
- Unexplained intellectual disability
If you’re planning a family and have concerns about genetic inheritance, this test provides valuable insights for your future.
Why Early Detection Matters for Your Family
Knowing your genetic status empowers you to:
- Make informed decisions about family planning
- Access appropriate medical care and interventions early
- Connect with specialist neurologists in Johannesburg, Cape Town, or Durban
- Participate in relevant support networks and research
- Reduce uncertainty and anxiety about your family’s health future
Early detection can significantly improve quality of life through timely interventions and specialised care.
Understanding Your Results with Compassion
We know waiting for genetic results can be stressful. That’s why we provide:
- Clear, easy-to-understand reports with expert interpretation
- Genetic counselling sessions to discuss your results
- Guidance on next steps and available resources
- Connection to neurological specialists across South Africa
- Ongoing support for your health journey
Our team ensures you never feel alone in understanding your results.
Transparent Pricing for Peace of Mind
| Service | Regular Price | Special Price |
|---|---|---|
| TMEM138 Gene Joubert Syndrome Type 16 Test | ZAR 6,700 | |
| Includes genetic counselling and comprehensive result interpretation | ||
This investment in your family’s health provides lifelong value through early detection and proper management.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Team: Working with qualified neurologists and genetic specialists
- Advanced Technology: Using NGS for highest accuracy in genetic testing
- Quick Turnaround: Results in 3-4 weeks with ongoing support
- Patient-First Approach: Compassionate care throughout your journey
Take Control of Your Family’s Health Today
Don’t let uncertainty dictate your family’s future. With our special pricing of ZAR 6,700, now is the perfect time to get the answers you deserve.
Book your test today and receive:
- Comprehensive genetic analysis using NGS technology
- Professional genetic counselling session
- Clear, actionable results in 3-4 weeks
- Nationwide accessibility across South Africa
- Peace of mind for your family’s health future
Contact us now to schedule your test and begin your journey to genetic clarity. Your family’s health is worth the investment.
