Understanding Noonan Syndrome Type 3: Your Path to Genetic Clarity
When you notice developmental delays, unusual facial features, or heart concerns in your child, the uncertainty can be overwhelming. Our KRAS Gene Noonan Syndrome Type 3 test provides the definitive answers you need to move forward with confidence and create the best possible care plan for your family.
What This Test Reveals About Your Health
This advanced genetic test specifically examines the KRAS gene using Next Generation Sequencing (NGS) technology – the gold standard in genetic analysis. The KRAS gene plays a crucial role in cell growth and development, and mutations in this gene are directly linked to Noonan Syndrome Type 3. By identifying these specific genetic changes, we can provide clear answers about your child’s condition and help guide their healthcare journey.
Is This Test Right for Your Family?
Consider this test if your child shows:
- Unusual facial features (wide-set eyes, low-set ears)
- Developmental delays or learning difficulties
- Heart abnormalities or murmurs
- Short stature or growth concerns
- Family history of Noonan Syndrome
- Unexplained bleeding or bruising tendencies
Early detection through genetic testing can make a significant difference in managing symptoms and improving quality of life.
Why Early Genetic Testing Matters
Getting a definitive diagnosis through our KRAS gene testing provides:
- Peace of Mind: End the uncertainty and know exactly what you’re dealing with
- Personalised Care: Create targeted treatment plans based on specific genetic findings
- Family Planning: Understand inheritance patterns for future family decisions
- Early Intervention: Access appropriate therapies and monitoring sooner
- Reduced Anxiety: Replace worry with actionable information and support
Understanding Your Results with Compassion
We know waiting for genetic results can be stressful. That’s why we provide:
- Clear, easy-to-understand reports with detailed explanations
- Access to genetic counselling to discuss your results
- Guidance on next steps and available resources
- Support in communicating findings to your healthcare team
- Ongoing access to our genetic specialists for questions
Our team is here to support you every step of the way, ensuring you feel confident and informed about your genetic health.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price |
|---|---|---|
| KRAS Gene Noonan Syndrome Type 3 Test | ZAR 6,700 | |
| Includes: Genetic testing, comprehensive report, and genetic counselling session | ||
Turnaround Time: 3-4 weeks
Sample Type: Blood, 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
- Medical Expertise: Specialised in pediatric genetic conditions
- Advanced Technology: Using NGS – the most accurate genetic testing method available
- Complete Support: Genetic counselling included with every test
- Proven Accuracy: Reliable results you can trust for important health decisions
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about Noonan Syndrome Type 3 delay your child’s care. Early detection through genetic testing can open doors to better management and improved outcomes.
Limited Time Offer: Save ZAR 2,650 on comprehensive KRAS gene testing. Early detection leads to better health outcomes – don’t wait to get the answers your family deserves.
