Find Clarity for Neurological Development Concerns
When your child shows signs of developmental challenges or you have a family history of neurological disorders, the uncertainty can feel overwhelming. Our OCLN Gene Band-like Calcification with Simplified Gyration and Polymicrogyria NGS Genetic DNA Test provides the definitive answers you need to make informed decisions about your family’s health journey.
Understanding Your OCLN Gene Test
This advanced genetic test examines the OCLN gene, which plays a crucial role in brain development and function. When this gene has specific mutations, it can lead to band-like brain calcification with simplified gyration and polymicrogyria – conditions that affect how the brain’s folds and structures develop. Our test uses Next Generation Sequencing (NGS) technology, the most accurate method available, to identify these genetic variations with precision.
Who Should Consider This Test?
This test is particularly important for families experiencing:
- Children showing developmental delays or neurological symptoms
- Family history of brain calcification disorders
- Unexplained seizures or epilepsy in childhood
- Motor skill development concerns
- Cognitive development challenges
- Previous abnormal brain imaging results
If you’ve been searching for answers about your child’s neurological health, this test can provide the clarity you need.
Why Early Detection Matters for Your Family
Getting a definitive diagnosis through genetic testing can transform your family’s healthcare journey:
- Peace of Mind: End the uncertainty and get clear answers
- Personalised Care: Enable targeted treatment and management strategies
- Family Planning: Understand inheritance patterns for future family decisions
- Early Intervention: Access appropriate therapies and support sooner
- Reduced Medical Costs: Avoid unnecessary tests and treatments
Understanding Your Results with Confidence
We know waiting for genetic test results can be anxiety-provoking. That’s why we include comprehensive genetic counselling as part of your testing process. Our specialists will:
- Create a detailed family pedigree to understand inheritance patterns
- Explain your results in clear, understandable language
- Discuss what the findings mean for your family’s health
- Provide guidance on next steps and available resources
- Connect you with appropriate specialists if needed
Your results will be ready within 3-4 weeks, and we’ll support you every step of the way.
Affordable, Comprehensive Genetic Testing
| Test Feature | Details | Value |
|---|---|---|
| Regular Price | ZAR 9,350 | Comprehensive analysis |
| Special Price | ZAR 6,700 | Limited time offer |
| Turnaround Time | 3-4 Weeks | Timely results |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | Flexible options |
| Included Services | Genetic Counselling & Family Pedigree | Complete support |
Considering the cost of ongoing specialist consultations and unnecessary treatments, this test represents significant long-term savings for your family’s health.
Why Trust Oracle Genomics?
We’re committed to providing South African families with accessible, reliable genetic testing:
- Nationwide Coverage: Available across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialised in pediatric genetic disorders
- Advanced Technology: Using NGS for maximum accuracy
- Patient-Focused: Empathetic support throughout your journey
- Proven Reliability: Trusted by healthcare professionals nationwide
Take the First Step Toward Clarity Today
Don’t let uncertainty about neurological development concerns continue to worry you. Our team is ready to help you get the answers your family deserves.
Limited Time Special: Book now to secure the ZAR 6,700 special price before it returns to ZAR 9,350. Every day of uncertainty is a day without the answers you need for your family’s health.
“The peace of mind we gained from getting definitive answers was priceless. We finally had a clear path forward for our son’s care.” – Previous Patient Family
