Find Clarity for Your Family’s Genetic Health Journey
When you’re worried about ventriculomegaly or cystic kidney disease running in your family, the uncertainty can feel overwhelming. We understand that waiting for answers about your genetic health creates anxiety and stress. Our CRB2 Gene Test provides the clarity and peace of mind you deserve, helping you take control of your family’s health future with confidence and accurate information.
Understanding Your CRB2 Gene Test
The CRB2 gene plays a crucial role in brain and kidney development. When mutations occur in this gene, it can lead to ventriculomegaly (enlarged brain ventricles) and cystic kidney disease. Our advanced Next Generation Sequencing (NGS) technology examines your DNA with exceptional precision, identifying even the smallest genetic variations that could impact your health.
This isn’t just a test – it’s a comprehensive health assessment that gives you and your healthcare provider the information needed to make proactive decisions about your care and management strategies.
Who Should Consider This Important Genetic Test?
This test is particularly important if you or your family members experience:
- Family history of ventriculomegaly or hydrocephalus
- Multiple family members with kidney cysts or kidney disease
- Unexplained developmental delays in children
- Previous pregnancies affected by brain or kidney abnormalities
- Planning for pregnancy with family history of these conditions
Early detection through genetic testing can provide valuable insights for family planning and proactive healthcare management.
Why Early Detection Matters for Your Family’s Health
Knowing your genetic status empowers you to:
- Make informed decisions about family planning
- Access appropriate monitoring and early intervention
- Reduce anxiety through clear understanding of risks
- Connect with specialists who understand your specific needs
- Participate in research and support communities
Many families find that genetic testing brings relief from uncertainty and provides a clear path forward for their healthcare journey.
Understanding Your Results with Compassion
We know that waiting for genetic test results can be stressful. That’s why we provide:
- Clear, easy-to-understand reports with your doctor
- Professional genetic counselling to explain your results
- Guidance on next steps and available resources
- Support in connecting with appropriate specialists
- Ongoing access to our genetic counselling team
Whether your results show a genetic variation or provide reassuring information, we’re here to support you every step of the way.
Affordable Genetic Testing for South African Families
| Test Details | Regular Price | Special Price |
|---|---|---|
| CRB2 Gene NGS Test | ZAR 6,700 | |
| Turnaround Time | 3-4 Weeks | |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card | |
| Included Services | Genetic Counselling & Family History Assessment | |
Consider the value: Early detection can save thousands in future healthcare costs while providing priceless peace of mind for your family.
Why South Africans Trust Oracle Genomics
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Accuracy Guaranteed: Advanced NGS technology for reliable results
- Patient-Focused Care: We understand the emotional journey of genetic testing
- Proven Track Record: Trusted by healthcare providers nationwide
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about your genetic health create unnecessary stress. Our caring team is ready to help you understand your family’s health risks and provide the answers you need.
Limited Time Offer: Special pricing of ZAR 6,700 available for a limited time only. Take action today to secure this valuable health investment for your family.
