Find Answers for Unexplained Joint and Bone Conditions
When your child experiences persistent joint laxity, unusual bone development, or recurrent fractures without clear cause, the uncertainty can be overwhelming. Our B3GALT6 Gene Test provides the clarity you’ve been searching for, offering definitive answers about spondyloepimetaphyseal dysplasia with joint laxity type 1 – a genetic condition affecting bone growth and joint stability.
Understanding Your B3GALT6 Genetic Test
This specialised test examines the B3GALT6 gene using advanced Next Generation Sequencing (NGS) technology to identify mutations that cause spondyloepimetaphyseal dysplasia with joint laxity type 1. This condition affects how bones develop in the spine, long bones, and joints, often leading to hypermobility and increased fracture risk.
Our comprehensive approach includes genetic counselling to help you understand family inheritance patterns and what the results mean for your child’s health journey.
Who Should Consider This Genetic Test?
This test is particularly important if your child shows:
- Unexplained joint hypermobility or looseness
- Delayed bone development or abnormal bone shape
- Recurrent fractures with minimal trauma
- Family history of similar bone or joint conditions
- Spinal abnormalities detected during growth
- Difficulty with mobility or physical activities
Early testing can provide crucial information for managing symptoms and preventing complications.
Why Early Detection Matters for Your Child’s Health
Getting answers through genetic testing transforms uncertainty into actionable health plans. With a confirmed diagnosis, you can:
- Develop targeted management strategies with your healthcare team
- Implement preventive measures to reduce fracture risk
- Access appropriate physical therapy and support services
- Make informed decisions about future family planning
- Connect with support communities and resources
- Reduce anxiety through clear understanding of the condition
Understanding Your Test Results
Our genetic counsellors will walk you through your results with compassion and clarity. We explain:
- What specific genetic changes were found (if any)
- How these changes affect bone and joint development
- Inheritance patterns and family implications
- Recommended next steps and specialist referrals
- Management strategies for improved quality of life
You’ll leave with a clear understanding and practical guidance for moving forward.
Affordable Genetic Testing with Clear Value
| Service | Regular Price | Special Price |
|---|---|---|
| B3GALT6 Gene Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Explanation | Included | |
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why Trust Oracle Genomics?
We bring medical excellence and compassionate care to genetic testing across South Africa:
- Nationwide Coverage: Serving patients in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
- Advanced Technology: Next Generation Sequencing with 99.9% accuracy
- Expert Team: Board-certified genetic specialists and counsellors
- Comprehensive Support: From testing to results explanation and beyond
- Patient-Focused: We understand the emotional journey of genetic testing
Take the First Step Toward Clarity Today
Don’t let uncertainty about your child’s bone and joint health continue. Our genetic testing provides the answers you need to make informed decisions and access appropriate care.
Book your test now while special pricing is available:
- Call our genetic counselling team for immediate assistance
- Schedule your appointment online for convenience
- Visit one of our nationwide collection centres
- Speak with your healthcare provider about referral
Early detection means earlier intervention and better outcomes. Take control of your family’s genetic health journey with Oracle Genomics.
