Find Clarity for Your Child’s Neurological Health Journey
When your child faces developmental challenges or unexplained neurological symptoms, the uncertainty can feel overwhelming. Our KCNH1 Gene Temple-Baraitser Syndrome NGS Genetic DNA Test provides the answers South African families need to move forward with confidence and clarity.
Understanding the KCNH1 Temple-Baraitser Syndrome Test
This advanced genetic test uses Next-Generation Sequencing (NGS) technology to examine the KCNH1 gene for mutations associated with Temple-Baraitser syndrome – a rare neurological condition that affects development and can cause intellectual disability, seizures, and distinctive physical features. Unlike basic genetic screenings, our comprehensive analysis provides definitive answers about this specific genetic condition.
Who Should Consider This Genetic Test?
This test is particularly important for families where a child shows:
- Unexplained developmental delays or intellectual disability
- Seizures or epilepsy that began in early childhood
- Distinctive facial features or physical characteristics
- Family history of similar neurological conditions
- Multiple specialists unable to provide a clear diagnosis
If your child has seen multiple doctors without getting clear answers, this genetic test could provide the breakthrough you need.
Why This Test Matters for Your Family’s Health
Getting a definitive genetic diagnosis offers profound benefits:
- Clear Treatment Direction: Understand the specific condition to guide medical management
- Family Planning Insights: Learn about inheritance patterns for future family planning
- Reduced Medical Uncertainty: End the diagnostic odyssey and multiple specialist visits
- Early Intervention Opportunities: Access appropriate therapies and support services sooner
- Peace of Mind: Replace uncertainty with understanding and a clear path forward
Understanding Your Test Results
We know genetic test results can feel overwhelming. That’s why every test includes genetic counselling to help you understand what your results mean for your child and family. Our specialists will:
- Explain your results in clear, understandable language
- Create a family pedigree chart to understand inheritance patterns
- Discuss next steps and available support resources
- Connect you with appropriate medical specialists in South Africa
- Provide ongoing support for your family’s journey
Transparent Pricing – Exceptional Value
| Test Feature | Details | Value |
|---|---|---|
| Regular Price | ZAR 9,350 | Comprehensive genetic analysis |
| Special Price | ZAR 6,700 | Limited time savings of ZAR 2,650 |
| Turnaround Time | 3-4 Weeks | Faster than many international labs |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | Multiple convenient options |
| Genetic Counselling | Included | Essential for understanding results |
Consider the value: This test could save you thousands in unnecessary specialist visits and provide answers that guide appropriate, cost-effective care.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialised in paediatric genetic conditions with South African context
- Advanced Technology: NGS technology provides superior accuracy over older methods
- Patient-First Approach: We understand the emotional journey of genetic testing
- Local Support: Genetic counselling tailored to South African healthcare systems
Take the First Step Toward Clarity Today
Don’t let uncertainty about your child’s health continue. With our special pricing of ZAR 6,700, now is the time to get the answers your family deserves.
Limited time offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) won’t last forever. Take action today to secure your family’s health clarity.
