Understanding Your Genetic Risk for Hemophilia A
Living with uncertainty about hemophilia A can be overwhelming, especially when you’re planning a family or have relatives affected by bleeding disorders. We understand the anxiety that comes with genetic concerns, which is why our Hemophilia A Common Mutation Screening offers clarity and peace of mind through advanced genetic analysis.
What This Test Detects
This specialised screening focuses on identifying the two most common genetic mutations responsible for hemophilia A – Factor VIII Intron 22 and Intron 1 Inversions. These specific genetic changes account for nearly half of all severe hemophilia A cases, making this test crucial for accurate diagnosis and family planning.
Using advanced End Point PCR technology, we analyse your DNA with precision and reliability, ensuring you receive results you can trust for making important health decisions.
Who Should Consider This Screening?
- Individuals with a family history of hemophilia or bleeding disorders
- Women considering pregnancy who have hemophilia in their family
- Parents concerned about passing genetic conditions to children
- Individuals experiencing unexplained bleeding or bruising
- Those with abnormal coagulation test results
- Couples planning families where hemophilia risk exists
If you recognise any of these situations in your life, this screening could provide the answers you need to move forward with confidence.
Why Early Detection Matters for Your Health
Knowing your genetic status empowers you to make informed decisions about your health and family planning. Early detection of hemophilia A mutations allows for:
- Proactive management of bleeding risks
- Informed family planning decisions
- Early intervention strategies for affected children
- Reduced anxiety through genetic certainty
- Better preparation for medical procedures
- Access to appropriate specialist care
Peace of mind is priceless when it comes to your family’s genetic health.
Understanding Your Results
We know waiting for genetic test results can be stressful. Our team provides clear, compassionate explanations of your findings:
- Positive Result: Indicates the presence of hemophilia A mutations – our genetic counsellors will guide you through next steps
- Negative Result: No common mutations detected – providing reassurance for you and your family
- Carrier Status: Important information for family planning and genetic counselling
Every result comes with professional guidance to help you understand what it means for your health and future.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| Hemophilia A Common Mutation Screening | ZAR 5,000 | ZAR 2,350 |
Price includes comprehensive analysis, detailed report, and professional result interpretation
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Working with qualified General Physicians and genetic specialists
- Accuracy Guarantee: Advanced End Point PCR technology ensures reliable results
- Quick Turnaround: Results within 10-11 days from sample receipt
- Patient-Focused Care: Empathetic support throughout your testing journey
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about hemophilia A affect your family planning or peace of mind. Our genetic screening provides the answers you need to make confident health decisions.
Limited Time Offer: Save ZAR 2,350 on your genetic screening. Early detection could save your family from unnecessary health concerns and provide the clarity needed for informed decisions.
Note: This test requires a Doctor’s prescription, except for surgery preparation, pregnancy cases, or international travel planning.
Nationwide Accessibility
We’re committed to making genetic testing accessible to all South Africans. With service points in major cities including Johannesburg, Cape Town, Durban, Pretoria, and surrounding areas, quality genetic screening is within your reach.
