Find Answers for Your Child’s Unexplained Symptoms
When your child experiences persistent skin rashes, joint swelling, or eye inflammation without clear cause, the uncertainty can be overwhelming. Our NOD2 Gene Blau Syndrome NGS Genetic DNA Test provides the clarity you need to understand these complex symptoms and take control of your family’s health journey.
Understanding the NOD2 Blau Syndrome Test
Blau syndrome is a rare genetic condition that typically appears in early childhood, causing inflammation in multiple body systems. Our advanced NGS (Next Generation Sequencing) technology examines the NOD2 gene with exceptional accuracy, identifying specific mutations that cause this condition. This isn’t just a test – it’s a pathway to understanding your child’s health at the genetic level.
Using either a simple blood sample or a single drop of blood on an FTA card, we analyse the genetic markers that could be affecting your child’s health. The process is straightforward, and our team ensures you’re comfortable every step of the way.
Is This Test Right for Your Child?
Consider this test if your child experiences:
- Unexplained skin rashes or granulomatous dermatitis
- Persistent joint pain, swelling, or arthritis
- Recurrent eye inflammation (uveitis)
- Family history of similar symptoms
- Multiple inflammatory symptoms without clear diagnosis
Many parents in Johannesburg, Cape Town, and Durban have found answers through genetic testing when traditional diagnostic methods provided incomplete information.
Why Early Detection Matters for Your Family
Getting a definitive diagnosis through genetic testing can transform your child’s health management:
- Targeted Treatment: Knowing the specific genetic cause allows for more effective, personalised treatment plans
- Family Planning: Understand inheritance patterns for future family decisions
- Peace of Mind: End the uncertainty and diagnostic odyssey
- Proactive Management: Early intervention can prevent complications and improve long-term outcomes
- Reduced Healthcare Costs: Avoid unnecessary tests and treatments by getting the right diagnosis sooner
Understanding Your Results with Confidence
We know waiting for genetic test results can be anxiety-provoking. That’s why we include comprehensive genetic counselling with every test. Our specialists will:
- Explain your results in clear, understandable language
- Discuss what the findings mean for your child’s health
- Create a pedigree chart to understand family inheritance patterns
- Provide guidance on next steps and management options
- Connect you with appropriate specialists if needed
You’ll never feel alone in interpreting your results – our team supports you throughout the entire process.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| NOD2 Blau Syndrome NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | INCLUDED | ||
| Family Pedigree Analysis | INCLUDED | ||
| Results Interpretation | INCLUDED | ||
Turnaround time: 3-4 weeks | Sample: Blood or Extracted DNA or One drop Blood on FTA Card
Why South Africans Trust Oracle Genomics
Nationwide Coverage
Available in Johannesburg, Cape Town, Durban, Pretoria, and across South Africa with convenient sample collection options
Medical Expertise
Our team includes genetic specialists with extensive experience in pediatric genetic conditions
Advanced Technology
Using NGS technology for the most accurate and comprehensive genetic analysis available
Patient-Centred Care
We understand the emotional journey of genetic testing and provide compassionate support throughout
Take the First Step Toward Answers Today
Don’t let uncertainty about your child’s symptoms continue. Early genetic testing can provide the clarity needed for proper management and improved quality of life.
Limited time special pricing: Save ZAR 2,650 while this offer lasts. Every day without answers is another day your child could be receiving targeted care.
