Understanding Your Risk for Osteogenesis Imperfecta Type 7
If you’re worried about brittle bones running in your family or have experienced unexplained fractures, the CRTAP Gene Test provides the clarity you need. This advanced genetic screening helps identify Osteogenesis Imperfecta Type 7, a rare bone disorder that affects bone strength and development. Many South African families live with uncertainty about inherited bone conditions – our test offers definitive answers and peace of mind.
What Does This Test Detect?
The CRTAP Gene Test uses Next Generation Sequencing (NGS) technology to examine the CRTAP gene for mutations associated with Osteogenesis Imperfecta Type 7. This condition, often called brittle bone disease, affects collagen production and bone mineralization. Our test provides comprehensive analysis of your genetic makeup to identify potential risk factors that could impact your bone health and that of your family members.
Who Should Consider This Test?
- Individuals with a family history of Osteogenesis Imperfecta or brittle bone disease
- Parents concerned about passing genetic conditions to their children
- People experiencing frequent fractures with minimal trauma
- Those with blue sclerae (the white part of eyes appearing blue)
- Individuals with dental abnormalities or hearing loss at young age
- Couples planning pregnancy with family history of bone disorders
- Children showing signs of bone fragility or growth delays
Why Early Detection Matters for Your Health
Identifying Osteogenesis Imperfecta Type 7 early can significantly improve quality of life. With proper diagnosis, you can access targeted treatments, implement preventive measures, and make informed family planning decisions. Early detection helps prevent unnecessary fractures, reduces pain and disability, and provides the opportunity for proactive bone health management. Knowing your genetic status empowers you to take control of your health journey.
Understanding Your Test Results
Your results will be clearly explained during your genetic counselling session. We provide comprehensive reports that detail whether CRTAP gene mutations were detected and what this means for your health. Our genetic counsellors will guide you through understanding the implications for you and your family members. Positive results don’t mean certain disease development – they indicate increased risk that can be managed with proper medical care and lifestyle adjustments.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price |
|---|---|---|
| CRTAP Gene Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Consider the long-term savings: Early detection can prevent costly medical treatments and hospitalizations related to bone fractures and complications.
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Conducted by qualified dermatologists and genetic specialists
- Advanced Technology: Utilizes NGS technology for 99.9% accuracy
- Comprehensive Support: Genetic counselling included with every test
- Quick Turnaround: Results in 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
Take the First Step Toward Bone Health Clarity
Don’t let uncertainty about genetic bone conditions control your life. Our CRTAP Gene Test provides the answers you need to make informed health decisions. With genetic counselling included and results in just 3-4 weeks, you can gain peace of mind about your family’s health future.
Early detection saves lives and improves quality of life. Don’t wait – take control of your genetic health today.
