Protect Your Child’s Bone Health with SNX10 Gene Testing
As a parent, watching your infant struggle with unexplained bone issues can be heartbreaking. When traditional tests don’t provide answers, our SNX10 Gene Osteopetrosis DNA Test offers the clarity South African families need. This specialised genetic test identifies malignant osteopetrosis of infancy – a serious condition that affects bone development and requires early detection for the best outcomes.
Understanding the SNX10 Gene Test
The SNX10 Gene Osteopetrosis Test uses advanced Next Generation Sequencing (NGS) technology to examine the SNX10 gene for mutations that cause malignant osteopetrosis in infants. This isn’t just another blood test – it’s a comprehensive genetic analysis that provides definitive answers about your child’s bone health condition.
Osteopetrosis, sometimes called “marble bone disease,” occurs when bones become overly dense and brittle. The malignant infantile form is particularly serious and can lead to complications if not identified early. Our test specifically targets the SNX10 gene variant, giving you precise information to guide treatment decisions.
Who Should Consider This Test?
This test is crucial for infants and families showing these concerning signs:
- Infants with unexplained fractures or brittle bones
- Family history of osteopetrosis or bone disorders
- Delayed growth or development milestones
- Vision or hearing problems in infancy
- Anaemia or other blood abnormalities
- Enlarged liver or spleen without clear cause
If your paediatrician has mentioned concerns about your child’s bone density or development, this test can provide the answers you need for proper care planning.
Why Early Detection Matters for Your Child’s Health
Identifying SNX10 gene mutations early can significantly impact your child’s quality of life:
- Timely Intervention: Early diagnosis allows for prompt treatment planning
- Family Planning: Understand genetic risks for future pregnancies
- Prevent Complications: Reduce risk of vision loss, hearing impairment, and severe anaemia
- Peace of Mind: Replace uncertainty with clear understanding
- Treatment Guidance: Inform decisions about bone marrow transplantation and other therapies
Understanding Your Results – Clear and Compassionate Guidance
We know waiting for genetic test results can be stressful. That’s why we provide:
- Comprehensive Report: Easy-to-understand results with clear explanations
- Genetic Counselling: Professional support to interpret findings
- Family Guidance: Help understanding inheritance patterns and risks
- Next Steps: Clear recommendations for follow-up care
- Ongoing Support: Access to our genetic specialists for questions
Your results will clearly indicate whether SNX10 gene mutations were detected and what this means for your child’s health management.
Transparent Pricing – Exceptional Value for Peace of Mind
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| SNX10 Gene Osteopetrosis NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
Turnaround Time: 3 to 4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Preparation: Clinical history and genetic counselling session included
Considering the potential lifelong impact of undiagnosed osteopetrosis, this test represents exceptional value for your child’s health future.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Specialised dermatology and genetic professionals
- Advanced Technology: Cutting-edge NGS technology for 99.9% accuracy
- Patient-Focused Care: Empathetic support throughout your testing journey
- Proven Reliability: Trusted by healthcare providers nationwide
Take the First Step Toward Answers Today
Don’t let uncertainty about your child’s bone health continue. Early detection of SNX10 gene mutations can make a life-changing difference.
Limited Time Offer: Special pricing of ZAR 6,700 available for immediate bookings. Regular price ZAR 9,350.
Our team is ready to support you through this important health decision. Contact us today to schedule your genetic counselling session and testing.
