Find Clarity About Hereditary Hearing and Kidney Conditions
When you notice hearing difficulties, neck abnormalities, or kidney concerns running in your family, the uncertainty can be overwhelming. Our SIX5 Gene Branchiootorenal Syndrome Type 2 test provides the definitive answers you need to protect your family’s health and plan for the future with confidence.
Understanding Your SIX5 Gene Test
Branchiootorenal (BOR) syndrome is an inherited condition that affects hearing, kidney development, and physical features. Our advanced Next-Generation Sequencing (NGS) technology examines your SIX5 gene with 99.9% accuracy, identifying mutations that could impact your health and your children’s future.
This isn’t just a test – it’s a comprehensive health assessment that includes genetic counselling to understand your complete family picture and provide personalised guidance.
Who Should Consider This Important Test?
This test is essential if you or your family members experience:
- Progressive hearing loss, especially starting in childhood
- Unusual neck cysts or skin tags
- Kidney abnormalities or recurrent urinary infections
- Ear malformations or hearing aid dependence
- Family history of similar hearing or kidney issues
- Planning pregnancy with concerns about hereditary conditions
Many South African families discover these symptoms run through generations without understanding the genetic connection.
Why Early Detection Matters for Your Family’s Health
Knowing your genetic status empowers you to:
- Prevent progressive hearing loss through early intervention
- Monitor kidney function and prevent serious complications
- Make informed family planning decisions
- Access appropriate medical care and support services
- Reduce anxiety through definitive answers
- Protect future generations through genetic counselling
Early detection can significantly improve quality of life and prevent costly medical complications down the line.
Understanding Your Results with Compassion
Our specialist ophthalmologists and genetic counsellors provide clear, compassionate explanations of your results. You’ll receive:
- Easy-to-understand report with plain language explanations
- Personalised consultation to discuss findings
- Actionable recommendations for next steps
- Family planning guidance if needed
- Connections to appropriate specialists
- Ongoing support throughout your health journey
No matter your results, you’ll have a clear path forward and professional support every step of the way.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| SIX5 Gene BOR Syndrome Test | ZAR 6,700 | ZAR 2,650 |
Your investment includes: Comprehensive genetic testing, genetic counselling session, family pedigree analysis, detailed results report, and specialist consultation.
Consider this: Early detection could prevent thousands in future medical costs and priceless improvements to your quality of life.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Specialist ophthalmologists overseeing your care
- Advanced Technology: NGS testing with 99.9% accuracy
- Genetic Counselling: Professional guidance throughout your journey
- Quick Turnaround: Results in 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple FTA card
Take Control of Your Family’s Health Today
Don’t let uncertainty about hereditary conditions create unnecessary anxiety. With our special pricing of ZAR 6,700, now is the perfect time to get the answers you deserve.
Limited Time Offer: This special pricing of ZAR 6,700 won’t last forever. Take the first step toward peace of mind and book your genetic counselling session today.
Your family’s health story deserves clarity. Let us help you write the next chapter with confidence and certainty.
