Understanding FILS Syndrome: Your Family’s Genetic Health Matters
When you’re concerned about genetic conditions affecting your children or family members, the uncertainty can be overwhelming. Our POLE Gene FILS Syndrome NGS Genetic DNA Test provides the clarity and answers you need to make informed decisions about your family’s health journey. Using cutting-edge next-generation sequencing technology, we offer precise detection of POLE gene mutations with exceptional accuracy.
What Does This Test Detect?
The POLE Gene FILS Syndrome test examines specific mutations in the POLE gene that are associated with FILS (Familial Intestinal Lipomatosis Syndrome). This comprehensive analysis helps identify genetic variations that may increase the risk of developing this rare condition, providing crucial information for early intervention and family planning.
Who Should Consider This Test?
- Families with a history of intestinal lipomatosis or related symptoms
- Parents concerned about genetic conditions in their children
- Individuals experiencing unexplained gastrointestinal symptoms
- Families planning pregnancy with genetic risk factors
- Those seeking clarity about inherited conditions in their family tree
Why Early Detection Matters for Your Family
Early identification of POLE gene mutations can significantly impact your family’s health outcomes. By understanding your genetic risk, you can:
- Access appropriate medical monitoring and early intervention
- Make informed decisions about family planning
- Reduce anxiety through definitive answers
- Connect with specialist healthcare providers
- Participate in targeted treatment approaches
Understanding Your Results with Expert Support
Your test results come with comprehensive genetic counselling from our certified specialists. We’ll help you understand what your results mean in clear, straightforward language, and provide guidance on next steps for your family’s healthcare journey. Our team ensures you never feel alone in interpreting your genetic information.
Transparent Pricing – No Hidden Costs
| Service | Regular Price | Special Price |
|---|---|---|
| POLE Gene FILS Syndrome NGS Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
All prices include VAT and professional interpretation
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Team: Certified genetic counsellors and medical specialists
- Advanced Technology: Next-generation sequencing with 99.9% accuracy
- Comprehensive Support: From testing to results interpretation
- Proven Track Record: Trusted by healthcare providers nationwide
Test Information
- Turnaround Time: 3 to 4 weeks
- Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
- Preparation: Clinical history and genetic counselling session required
- Methodology: Next-Generation Sequencing (NGS) Technology
- Specialty: Pediatrics and Family Genetics
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about genetic conditions affect your family’s peace of mind. Our POLE Gene FILS Syndrome test provides the answers you need with professional support every step of the way.
Limited Time Offer: Save ZAR 2,650 on comprehensive genetic testing with included counselling.
