Find Clarity About Your Heart Health with FBN1 Marfan Syndrome Genetic Testing
When you’re experiencing unexplained symptoms or have a family history of connective tissue disorders, the uncertainty can be overwhelming. Our FBN1 Gene Marfan Syndrome NGS Genetic DNA Test provides the answers you need to protect your heart health and plan for the future with confidence.
Understanding Your FBN1 Genetic Test
The FBN1 gene provides instructions for making fibrillin-1, a protein essential for connective tissue strength and elasticity. When mutations occur in this gene, it can lead to Marfan syndrome – a condition that affects the heart, blood vessels, eyes, and skeletal system. Our advanced Next Generation Sequencing (NGS) technology examines your FBN1 gene with 99.9% accuracy, identifying even the smallest genetic variations that could impact your health.
Who Should Consider This Genetic Test?
This test is particularly important if you experience:
- Tall, slender build with long arms, legs, and fingers
- Family history of Marfan syndrome or sudden cardiac death
- Chest pain, heart palpitations, or shortness of breath
- Vision problems or lens dislocation
- Joint hypermobility or frequent joint pain
- Spinal curvature (scoliosis) or chest wall deformities
- Aortic enlargement or heart valve issues
Early detection through genetic testing can be life-saving, especially for preventing aortic dissection – a medical emergency.
Why This Test Matters for Your Health Journey
Getting tested provides more than just answers – it gives you peace of mind and a clear path forward:
- Early Intervention: Detect Marfan syndrome before serious complications develop
- Family Planning: Understand inheritance risks for future generations
- Personalised Care: Work with cardiologists to create targeted treatment plans
- Reduced Anxiety: Replace uncertainty with actionable information
- Preventative Measures: Implement lifestyle changes and monitoring protocols
Understanding Your Test Results
We make understanding your results straightforward and supportive:
- Positive Result: Indicates an FBN1 gene mutation. Our genetic counsellors will explain what this means and connect you with specialist cardiologists for comprehensive care management.
- Negative Result: No FBN1 mutation detected. This provides reassurance, though continued monitoring may be recommended based on clinical symptoms.
- Variant of Uncertain Significance: Rare genetic changes with unknown impact. We provide ongoing monitoring and re-evaluation as research advances.
Every result includes a detailed consultation with our genetic specialists to ensure you fully understand your genetic profile and next steps.
Transparent Pricing – Your Health Investment
| Service | Regular Price | Special Price |
|---|---|---|
| FBN1 Marfan Syndrome NGS Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Consultation | Included | |
Consider this: Early detection of Marfan syndrome can prevent emergency heart surgery costing ZAR 200,000+ and potentially save your life.
Why Thousands of South Africans Trust Oracle Genomics
- Nationwide Coverage: Convenient testing available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by specialist cardiologists and genetic counsellors
- Advanced Technology: NGS sequencing ensures highest accuracy standards
- Complete Support: From sample collection to results explanation, we’re with you every step
- Rapid Turnaround: Results typically within 3-4 weeks
- Multiple Sample Options: Blood draw, extracted DNA, or simple finger-prick blood spot
Take the First Step Toward Heart Health Clarity
Don’t let uncertainty about your genetic health create unnecessary stress. Our compassionate team is ready to help you understand your risk and take proactive steps toward better health.
Limited Time Offer: Book your FBN1 Marfan Syndrome test today and save ZAR 2,650 while gaining priceless peace of mind about your heart health future.
