Understanding RAB39B Gene X-Linked Intellectual Disability: Your Path to Clarity
When intellectual disability runs in families, particularly affecting males, the uncertainty can be overwhelming. Our RAB39B gene test provides the answers you need to understand the genetic factors behind X-linked intellectual disability type 72. Using cutting-edge Next Generation Sequencing (NGS) technology, we offer precise, reliable results that can transform your family’s healthcare journey.
What This Test Reveals About Your Genetic Health
The RAB39B gene plays a crucial role in brain development and function. Mutations in this gene can lead to X-linked intellectual disability type 72, a condition that primarily affects males and can be passed through female carriers. Our test doesn’t just identify the presence of mutations – it provides a comprehensive understanding of your genetic risk factors, helping you make informed decisions about family planning and healthcare management.
Who Should Consider This Genetic Test?
This test is particularly important for families experiencing:
- Multiple cases of intellectual disability affecting male family members
- Unexplained developmental delays in boys
- Family history suggesting X-linked inheritance patterns
- Concerns about carrier status in female family members
- Planning for future pregnancies with known family history
If you’ve noticed these patterns in your family across generations, genetic testing can provide the clarity needed for proactive healthcare planning.
Why Early Detection Matters for Your Family’s Future
Understanding your genetic profile offers profound benefits:
- Peace of Mind: Eliminate uncertainty about genetic risks
- Informed Family Planning: Make confident decisions about future pregnancies
- Early Intervention: Access appropriate support and therapies sooner
- Carrier Identification: Understand risks for female family members
- Healthcare Guidance: Work with specialists to develop targeted care plans
Early detection through genetic testing can significantly improve quality of life and healthcare outcomes.
Understanding Your Test Results: Clear, Compassionate Guidance
Our genetic counsellors provide comprehensive support throughout your testing journey. We help you:
- Create detailed family pedigree charts to understand inheritance patterns
- Interpret complex genetic information in understandable terms
- Connect with appropriate medical specialists for ongoing care
- Develop family-specific management strategies
- Access resources and support networks
You’ll never face your results alone – our team ensures you have the support and understanding needed to move forward confidently.
Transparent Pricing – Exceptional Value for Peace of Mind
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| RAB39B Gene X-Linked Intellectual Disability Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or Blood on FTA Card
Consider the long-term value: Early genetic insights can prevent years of uncertainty and guide appropriate medical care that improves quality of life.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
- Expert Genetic Counselling: Pre-test sessions to understand your family history thoroughly
- Advanced NGS Technology: Most accurate genetic testing available
- Neurology Specialists: Results reviewed by experienced neurological geneticists
- Comprehensive Support: From initial consultation through result interpretation
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about genetic risks cloud your family’s future. Our special pricing of ZAR 6,700 makes this crucial testing more accessible than ever. With convenient testing locations across South Africa and expert genetic counselling support, you can approach your family’s health with confidence and clarity.
Limited Time Offer: Special pricing of ZAR 6,700 available for immediate bookings. Regular price ZAR 9,350.
