Find Clarity for Your Child’s Health Journey
When you’re concerned about developmental delays or neurological symptoms in your child, the uncertainty can be overwhelming. Our ERCC6 Gene Cerebrooculofacioskeletal Syndrome Type 1 test provides the answers you need to understand your child’s genetic health and plan for their future with confidence.
Understanding the ERCC6 COFS Syndrome Test
This advanced genetic test examines the ERCC6 gene, which plays a crucial role in DNA repair. When this gene has specific changes, it can lead to Cerebrooculofacioskeletal Syndrome Type 1 – a rare genetic condition affecting brain development, eye function, facial features, and skeletal growth.
Using Next-Generation Sequencing (NGS) technology, we analyse your DNA with exceptional accuracy, providing reliable results that help guide medical decisions and family planning.
Who Should Consider This Test?
- Children showing developmental delays or neurological symptoms
- Families with a history of COFS Syndrome or similar conditions
- Parents planning future pregnancies after having an affected child
- Individuals with unexplained neurological or developmental concerns
- Families seeking genetic clarity for better healthcare planning
If your child experiences symptoms like microcephaly (small head size), eye abnormalities, joint contractures, or developmental regression, this test could provide essential answers.
Why Early Detection Matters for Your Family
Getting the right diagnosis early can transform your child’s healthcare journey. With accurate genetic information, you can:
- Access appropriate medical care and interventions sooner
- Connect with specialists who understand the condition
- Make informed decisions about family planning
- Reduce the stress of uncertainty and multiple doctor visits
- Join support communities with families facing similar challenges
Understanding Your Results with Compassion
We know waiting for genetic test results can be anxiety-provoking. That’s why we provide:
- Clear, easy-to-understand reports with professional interpretation
- Genetic counselling sessions to help you understand the implications
- Guidance on next steps and available support resources
- Ongoing access to our medical team for questions
- Connection to South African specialists familiar with genetic conditions
Our team is here to support you through every step of the process.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| ERCC6 COFS Syndrome NGS Test | ZAR 6,700 |
Your investment includes:
- Comprehensive genetic analysis using NGS technology
- Professional genetic counselling session
- Detailed results report with medical interpretation
- 3-4 week turnaround time
- Multiple sample options (blood, DNA, or FTA card)
Why South African Families Trust Oracle Genomics
Nationwide Coverage
Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
Medical Expertise
Specialised in paediatric genetic testing with South African healthcare experience
Advanced Technology
Using latest NGS technology for highest accuracy in genetic analysis
Patient Support
Comprehensive genetic counselling and ongoing medical guidance
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about your child’s health continue. Early detection through genetic testing can provide the answers you need to make informed decisions and access the right support.
Limited time special pricing: Save ZAR 2,650 on comprehensive genetic testing with included counselling.
“Getting the right diagnosis helped us find the right support and therapies for our daughter. The genetic counselling made all the difference.” – Parent from Cape Town
