Take Control of Your CLL Journey with Advanced Genetic Testing
Living with chronic lymphocytic leukaemia can feel overwhelming, but understanding your genetic profile brings clarity and confidence. Our CLL Mutations Detection Panel 1 is specifically designed to provide the critical genetic information you and your oncologist need to make informed treatment decisions.
What This Test Reveals About Your CLL
This comprehensive panel examines 8 crucial genetic markers that directly impact your treatment response and disease progression. Using advanced PCR-MLPA technology, we analyse:
- 17p deletion – Associated with treatment resistance
- 11q deletion – Linked to aggressive disease progression
- Trisomy 12 – Common chromosomal abnormality in CLL
- 13q14 deletion – Often indicates better prognosis
- Chromosome 2p gain – Emerging prognostic marker
- 6q deletion – Associated with disease transformation
- 8p loss & 8q amplification – Important for risk stratification
- 9p21 loss – Tumor suppressor gene deletion
Who Should Consider This Genetic Panel?
This test is essential if you’re experiencing:
- Unexplained fatigue that doesn’t improve with rest
- Persistent swollen lymph nodes in neck, armpits, or groin
- Frequent infections or slow recovery from illness
- Unexplained weight loss or night sweats
- Family history of blood cancers or leukaemia
- Recent CLL diagnosis requiring treatment planning
- Monitoring disease progression or treatment response
Early genetic profiling can significantly impact your treatment success and quality of life.
Why Genetic Testing Matters for Your CLL Management
Understanding your genetic profile transforms uncertainty into actionable information:
- Personalised Treatment – Match therapies to your specific genetic mutations
- Prognostic Clarity – Understand your disease’s likely progression pattern
- Treatment Timing – Determine when to start or change therapies
- Clinical Trial Eligibility – Access targeted therapies based on genetic markers
- Peace of Mind – Replace uncertainty with clear, actionable information
- Family Planning – Understand potential hereditary factors
Understanding Your Results with Confidence
Your comprehensive report will clearly explain each genetic finding in patient-friendly language. Our medical team ensures you understand:
- What each mutation means for your specific situation
- How results impact treatment options and timing
- Next steps for discussion with your oncologist
- Monitoring recommendations based on your genetic profile
- Support resources available through your healthcare journey
No medical jargon – just clear, actionable information you can use immediately.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| CLL Mutations Detection Panel 1 | R1,700 | R800 |
Turnaround Time: Sample by Monday 11am, Results by Saturday
Sample Required: 4mL whole blood from lavender top EDTA tube
Mandatory: Completed Genomics Clinical Information Requisition Form (Form 20)
Why South Africans Trust Oracle Genomics
- Nationwide Coverage – Accessible testing in Johannesburg, Cape Town, Durban, Pretoria and nationwide
- Medical Expertise – Developed and interpreted by specialist oncologists
- 99.9% Accuracy – State-of-the-art PCR-MLPA technology
- Rapid Results – Comprehensive report within 5 days
- Patient Support – Clear result explanations and guidance
- Quality Assurance – International standard laboratory protocols
Take the First Step Toward Clarity Today
Don’t let uncertainty dictate your health journey. With genetic insights costing less than many monthly medical expenses, this test provides invaluable information for your treatment decisions.
Limited Time Offer: Save R800 on comprehensive genetic profiling
Convenient Nationwide Access: Testing available across South Africa
Fast Results: Get answers within 5 days to inform your next doctor’s appointment
Your genetic profile holds the key to personalised CLL treatment. Book your R1,700 CLL Mutations Detection Panel today and transform uncertainty into actionable health information.
Have questions? Call our genetic counselling team for personalised guidance.
