Understanding FKBP10 Gene Osteogenesis Imperfecta Type 11 Testing
If you or your loved ones experience frequent bone fractures, dental problems, or hearing loss that runs in the family, you understand the constant worry that comes with these symptoms. Osteogenesis Imperfecta Type 11, caused by mutations in the FKBP10 gene, is a genetic condition that affects bone strength and quality. Our comprehensive genetic test provides the answers you need to take control of your bone health journey.
What This Test Detects
This advanced NGS (Next-Generation Sequencing) test specifically examines the FKBP10 gene for mutations associated with Osteogenesis Imperfecta Type 11. The FKBP10 gene plays a crucial role in collagen formation and bone development. When this gene contains specific mutations, it can lead to brittle bones that fracture easily, dental abnormalities, and progressive hearing loss. By identifying these genetic variations, we can provide clarity about your condition and guide appropriate management strategies.
Who Should Consider This Test
This genetic test is particularly important if you or your family members experience:
- Frequent bone fractures with minimal trauma
- Family history of brittle bone disease
- Dental problems including discoloured or brittle teeth
- Progressive hearing loss starting in childhood or young adulthood
- Short stature or bone deformities
- Blue or grey tint to the whites of the eyes
- Planning pregnancy with family history of bone disorders
Why Early Detection Matters for Your Health
Understanding your genetic risk for Osteogenesis Imperfecta Type 11 empowers you to make informed health decisions. Early detection allows for:
- Proactive bone health management and fracture prevention
- Personalised treatment plans with your healthcare provider
- Informed family planning decisions
- Early intervention for dental and hearing complications
- Peace of mind through accurate diagnosis
- Access to appropriate support services and resources
Understanding Your Test Results
We understand that waiting for genetic test results can be anxiety-provoking. Our team provides clear, compassionate explanation of your results, including:
- Detailed report of any FKBP10 gene mutations detected
- Explanation of what the results mean for your health
- Guidance on next steps and management options
- Referral to appropriate specialists if needed
- Genetic counselling to help you understand inheritance patterns
Comprehensive Pricing Information
| Service | Regular Price | Special Price |
|---|---|---|
| FKBP10 Gene Test | ZAR 9,350 | ZAR 6,700 |
| Turnaround Time | 3-4 Weeks | |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | |
Nationwide Coverage and Trust Elements
Oracle Genomics provides reliable genetic testing services across South Africa, with convenient locations in Johannesburg, Cape Town, Durban, and Pretoria. Our commitment to accuracy and patient care includes:
- State-of-the-art NGS technology for precise results
- Experienced genetic specialists and counsellors
- Comprehensive pre-test genetic counselling sessions
- Strict confidentiality and data protection
- Clear communication throughout the testing process
Take the First Step Toward Bone Health Clarity
Don’t let uncertainty about your bone health continue to cause worry. Early detection through genetic testing can provide the answers you need to manage your health proactively. Our special pricing of ZAR 6,700 makes this comprehensive testing more accessible than ever.
Book your genetic counselling session today to discuss whether FKBP10 gene testing is right for you. Our team is ready to support you through every step of this important health journey.
Contact Oracle Genomics now to schedule your appointment and take control of your bone health future.
