Take Control of Your Genetic Health Journey
We understand that thinking about inherited diseases can feel overwhelming. Many South Africans worry about conditions that run in their families – from heart conditions to metabolic disorders. Our Complete Inherited Disease Panel provides the clarity and peace of mind you deserve, helping you make informed decisions about your health and your family’s future.
Understanding Your Complete Inherited Disease Panel
This comprehensive genetic screening uses Next Generation Sequencing (NGS) technology to analyse your DNA for over 400 inherited conditions. Think of it as a detailed roadmap of your genetic health – identifying potential risks before they become health concerns. The test examines genes associated with cardiovascular conditions, metabolic disorders, neurological conditions, and many other inherited health risks that affect South African families.
Who Should Consider This Genetic Screening?
- Individuals with a family history of inherited diseases
- Couples planning to start a family
- People experiencing unexplained symptoms that might have genetic origins
- Anyone wanting proactive health insights for better lifestyle planning
- Individuals from communities with higher prevalence of specific genetic conditions
If you’ve ever wondered “could this condition be inherited?” or “what health risks might I pass to my children?” – this panel provides the answers you need.
Why This Matters for Your Health Journey
Early detection through genetic screening can be life-changing. Knowing your genetic risks allows you and your healthcare provider to:
- Implement preventive measures and early interventions
- Make informed family planning decisions
- Reduce anxiety about unknown health risks
- Create personalised health monitoring plans
- Potentially prevent or delay the onset of conditions
Many of our patients describe the relief of finally having answers after years of uncertainty about their family’s health patterns.
Understanding Your Results with Confidence
We know waiting for genetic results can create anxiety. That’s why our genetic counsellors provide clear, compassionate explanations of your findings. You’ll receive:
- A comprehensive report written in understandable language
- Access to genetic counselling to discuss your results
- Guidance on next steps and preventive measures
- Support in sharing results with your healthcare provider
- Resources for managing any identified risks
Remember: Most genetic variations don’t guarantee disease – they indicate increased risk that can often be managed effectively with early awareness.
Invest in Your Genetic Health Today
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| Complete Inherited Disease Panel | ZAR 16,000 | ZAR 12,000 | ZAR 4,000 |
Consider this: The cost of managing one undetected inherited condition can far exceed this investment in proactive screening. Many medical aid schemes recognise the value of preventive genetic testing.
Why South Africans Trust Oracle Genomics
- Nationwide Coverage: Convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests conducted under medical supervision with doctor’s prescription when required
- Advanced Technology: 99.9% accuracy using latest NGS sequencing methods
- Fast Turnaround: Results in 4-6 weeks with ongoing support
- Confidential Service: Your genetic information is protected with strict privacy protocols
Ready to Unlock Your Genetic Health Insights?
Don’t let uncertainty about inherited health risks create unnecessary anxiety. Take the first step toward proactive health management today.
Limited Time Offer: Book your Complete Inherited Disease Panel at the special price of ZAR 12,000 before this offer ends. Early detection could make all the difference for your family’s health legacy.
“Many patients tell us they wish they had this information years earlier. Don’t wait for symptoms to appear – knowledge is your most powerful health tool.” – Oracle Genomics Medical Team
Test Specifications:
- Turnaround Time: 4-6 weeks
- Sample Type: Amniotic fluid / Chorionic villi / Peripheral blood
- Components: Sterile container / Sterile Normal Saline Container / EDTA Vacutainer
- Preparation: Doctor’s prescription required (not applicable for surgery, pregnancy, or travel abroad cases)
- Specialty: General Physician
- Method: Next Generation Sequencing (NGS)
