Take Control of Your Iron Health with Hemochromatosis Genetic Testing
Are you experiencing unexplained fatigue, joint discomfort, or noticing unusual skin changes? These could be signs of hemochromatosis – a genetic condition that causes your body to store dangerous levels of iron. Our Hemochromatosis Detection HFE Genotyping test provides the clarity you need to protect your long-term health.
Understanding Hemochromatosis Genetic Testing
Hemochromatosis is a hereditary disorder where your body absorbs excessive iron from food, leading to iron overload that can damage your liver, heart, and other organs. Our HFE Genotyping test examines three specific genetic mutations (H63D, S65D, C282Y) that are responsible for most cases of hereditary hemochromatosis. Using advanced Real Time PCR technology, we provide accurate, reliable results that help identify your genetic risk before symptoms become severe.
Who Should Consider This Test?
This test is particularly important if you experience:
- Unexplained chronic fatigue or weakness
- Joint pain, especially in hands and fingers
- Abdominal pain or discomfort
- Bronze or grey skin discolouration
- Irregular heart rhythms
- Family history of liver disease or hemochromatosis
- Elevated iron levels in previous blood tests
Early detection is crucial – many people live with hemochromatosis for years without realizing it, allowing iron to accumulate and cause permanent damage.
Why Early Detection Matters for Your Health
Knowing your genetic status empowers you to:
- Prevent organ damage – Early treatment can prevent iron from damaging your liver, heart, and pancreas
- Avoid complications – Reduce risk of developing diabetes, arthritis, or heart failure
- Take proactive measures – Simple treatments like therapeutic phlebotomy can manage iron levels effectively
- Protect family members – Genetic information helps assess risk for children and relatives
- Gain peace of mind – Either rule out the condition or create an effective management plan
Understanding Your Test Results
We make understanding your results simple and stress-free:
- Negative Result: No detected mutations – significantly reduced risk of hereditary hemochromatosis
- Single Mutation Carrier: You carry one copy of a mutation – unlikely to develop symptoms but important for family planning
- Double Mutation (Homozygous): Two copies of mutations – high risk for developing hemochromatosis, requiring medical management
- Compound Heterozygous: Different mutations from each parent – moderate to high risk requiring monitoring
Every result includes clear explanations and recommended next steps from our medical team.
Affordable Genetic Testing for Peace of Mind
| Test Option | Regular Price | Special Price | Savings |
|---|---|---|---|
| Hemochromatosis HFE Genotyping | ZAR 2,350 | ZAR 1,000 |
Consider the value: Early detection can prevent thousands in future medical costs from complications like liver cirrhosis or diabetes.
Why Trust Oracle Genomics?
- Nationwide Coverage – Convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise – Tests reviewed by qualified hematologists and oncologists
- Advanced Technology – Real Time PCR methodology ensures 99.9% accuracy
- Fast Turnaround – Samples collected Mon/Thu by 9am, reports delivered Wed/Sat
- Complete Support – Our team guides you through every step, from testing to understanding results
Take the First Step Toward Better Health Today
Don’t let uncertainty about your iron health cause unnecessary worry. Our Hemochromatosis Detection test provides the answers you need to make informed decisions about your health.
Limited Time Offer: Save ZAR 1,000 on your Hemochromatosis genetic testing. Early detection could save you from serious health complications down the line.
Testing requires: 3 mL whole blood in Lavender Top EDTA tube (shipped refrigerated) and completed Genomics Clinical Information Form 20.
