Find Clarity for Your Child’s Health Journey
When your child faces unexplained developmental delays or neurological symptoms, the uncertainty can be overwhelming. Our COG1 Gene Glycosylation Disorder Type 2G test provides the answers South African families need to understand complex genetic conditions and plan for the future with confidence.
Understanding the COG1 Gene Test
This specialised genetic test examines the COG1 gene using advanced Next-Generation Sequencing (NGS) technology to identify mutations that cause Glycosylation Disorder Type 2G. This condition affects how the body processes sugars for protein function, which can impact multiple body systems, particularly neurological development.
Unlike basic genetic screenings, our comprehensive analysis provides detailed information about specific genetic variations, giving you and your healthcare provider the precise data needed for accurate diagnosis and management.
Who Should Consider This Test?
This test is particularly important for families experiencing:
- Unexplained developmental delays in infants or children
- Neurological symptoms without clear diagnosis
- Family history of metabolic or genetic disorders
- Multiple unexplained health issues affecting different body systems
- Previous children with similar symptoms
If your child has shown signs like poor growth, feeding difficulties, or unusual neurological findings, this test could provide the missing piece to their health puzzle.
Why Early Detection Matters for Your Family
Getting answers through genetic testing can transform your family’s health journey:
- Peace of Mind: End the uncertainty and know exactly what you’re dealing with
- Targeted Treatment: Guide healthcare providers toward appropriate interventions
- Family Planning: Understand inheritance patterns for future family decisions
- Early Intervention: Access specialised care sooner for better outcomes
- Reduced Medical Costs: Avoid unnecessary tests and treatments through accurate diagnosis
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 your genetic counsellor
- Comprehensive explanation of what the results mean for your family
- Guidance on next steps and available support resources
- Connection to specialists who understand genetic conditions
- Ongoing support throughout your health journey
Our team ensures you never feel alone in understanding and managing genetic health information.
Transparent Pricing for South African Families
| Service | Regular Price | Special Price | Turnaround Time |
|---|---|---|---|
| COG1 Gene Glycosylation Disorder Test | ZAR 9,350 | ZAR 6,700 | 3-4 Weeks |
Includes genetic counselling session and comprehensive result interpretation
Why South African Families Trust Oracle Genomics
Nationwide Accessibility
Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
Advanced Technology
Using cutting-edge NGS technology for the most accurate results
Expert Genetic Counselling
Included with every test to ensure you understand your results
Simple Sample Collection
Blood, extracted DNA, or simple blood spot on FTA card options available
Take the First Step Toward Answers Today
Don’t let uncertainty about your child’s health continue. Our genetic counsellors are ready to help you understand if this test is right for your family and guide you through the simple process.
Limited time special pricing: Save ZAR 2,650 on this comprehensive genetic analysis. Early detection can make all the difference in managing genetic conditions effectively.
