Why Test for Haemochromatosis? (€150)
Haemochromatosis is a common genetic disorder that causes your body to absorb and store too much iron, potentially leading to serious health issues like liver damage, heart disease, diabetes, and arthritis if left undiagnosed.
Often referred to as the “Celtic curse,” haemochromatosis is especially prevalent in people of Irish and northern European descent. Many people carry the gene without knowing it, and early symptoms such as fatigue, joint pain, or abdominal discomfort are often overlooked or misattributed to other conditions.
A genetic blood test costing €150 can determine whether you carry the HFE gene mutation that causes haemochromatosis—enabling early intervention and long-term health protection.
You do not need to fast for this test, but we recommend arriving warm and well hydrated to make your blood draw as easy and comfortable as possible. Results are typically available within 7 days.
- What a Haemochromatosis Genetic Test Reveals:
- Gene Mutation Detection: Identifies mutations in the HFE gene (typically C282Y and H63D) associated with hereditary haemochromatosis.
- Risk Assessment: Determines if you're a carrier, at risk of developing iron overload, or already predisposed to related health complications.
- Early Detection Advantage: Enables early intervention before symptoms progress or organ damage occurs.
- Family Health Insight: Helps family members assess their risk and consider screening as well.
- Who Should Get Tested?
- Individuals with a family history of haemochromatosis or unexplained iron overload
- People with symptoms like chronic fatigue, joint pain, liver abnormalities, or skin bronzing
- Men over 30 and post-menopausal women (when iron levels tend to accumulate)
- Anyone with elevated ferritin or transferrin saturation in routine bloodwork
- Individuals of Irish or northern European ancestry