2026 Workshop Programme

Iron deficiency and low ferritin are most common in women and children, while men are more susceptible to iron overload. Both conditions can go undiagnosed without proper assessment. Genetic factors play a key role: HFE gene variants can reduce hepcidin, causing iron accumulation and silent organ damage, whereas TMPRSS6 variants can increase hepcidin, limiting absorption and contributing to deficiency. Genetic testing enables early identification of at-risk individuals and guide personalised interventions to prevent life-limiting complications from iron imbalance.