Understanding Saethre-Chotzen Syndrome: Your Family’s Genetic Health Matters
When you notice unusual skull shape development or facial features in your child, the uncertainty can be overwhelming. Our FGFR2 gene test provides the clarity you need to understand Saethre-Chotzen syndrome risks and make informed decisions about your family’s health journey.
What This Test Reveals About Your Genetic Health
This advanced NGS (Next Generation Sequencing) test specifically examines the FGFR2 gene for mutations that cause Saethre-Chotzen syndrome – a condition affecting skull bone fusion and facial development. Unlike basic genetic screens, our comprehensive analysis provides detailed insights into your specific genetic makeup, helping identify inherited patterns that could affect future generations.
When Should You Consider This Genetic Test?
This test is particularly important if your child shows:
- Unusual skull shape or premature fusion of skull bones
- Distinctive facial features including drooping eyelids
- Finger or toe abnormalities (syndactyly)
- Family history of craniosynostosis conditions
- Developmental delays alongside physical symptoms
Early testing can provide crucial information for treatment planning and family health decisions.
Why Early Detection Matters for Your Family
Getting tested offers significant advantages:
- Peace of Mind: Eliminate uncertainty about your child’s condition
- Early Intervention: Access appropriate treatments and specialists sooner
- Family Planning: Understand inheritance risks for future children
- Treatment Guidance: Help doctors create targeted care plans
- Genetic Counselling: Professional support for understanding results
Understanding Your Test Results with Confidence
We know waiting for genetic results can be stressful. Our comprehensive report includes:
- Clear explanation of FGFR2 gene findings in simple language
- Detailed discussion with our genetic counsellors
- Family pedigree analysis to understand inheritance patterns
- Recommendations for next steps and specialist referrals
- Ongoing support for questions and concerns
Your results will be thoroughly explained by our expert team, ensuring you feel supported every step of the way.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| FGFR2 Saethre-Chotzen NGS Test | ZAR 6,700 | |
| Includes Genetic Counselling | ✓ Included | |
| Turnaround Time | 3-4 Weeks | |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | |
This comprehensive package represents exceptional value, including professional genetic counselling that typically costs ZAR 2,000-3,000 separately.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and nationwide
- Medical Expertise: Specialist paediatric genetic testing with 99.9% accuracy
- Patient-First Approach: Empathetic support throughout your testing journey
- Advanced Technology: Latest NGS sequencing for comprehensive results
- Proven Track Record: Trusted by healthcare professionals across South Africa
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about your family’s genetic health create unnecessary stress. Early detection through our FGFR2 test can provide the answers you need to move forward with confidence.
Limited Time Offer: This special pricing includes complete genetic counselling and may not be available indefinitely. Secure your family’s health future while this comprehensive package remains at ZAR 6,700.
