24/02/2026
Iron deficiency is the most common nutritional deficiency worldwide, yet its impact is often underestimated. It affects women and children, more frequently than men, and its consequences span from increased risk of neurodevelopmental conditions, through hormonal and immune imbalances, to osteoporosis and cognitive decline.
Genetic variants in the TMPRSS6 gene, which regulates hepcidin and iron absorption, can significantly increase susceptibility to deficiency and reduce response to oral iron. But it is most often not so simple. A true nutrigenetics approach should consider genes and environmental factors that impact absorption, metabolism and depletion of copper – for ceruloplasmin synthesis, as well as magnesium and Vitamin A.
This case study style webinar will highlight why proactive screening — particularly in women and children — is essential, and why nutrigenetic testing is a critical component of a functional medicine approach to prevention and early intervention.
This is 1 of a 2 part series on Iron and Nutrigenetics. Part 2 on Iron overload (haemachromatosis) will take place on 13 April.
Join us from 6pm on 9 March. Free to register.
Register now for Iron Deficiency: Hidden Consequences Across the Lifespan on crowdcast, scheduled to go live on March 9, 2026, 06:00 PM GMT.