Prevalence of narcolepsy in patients with H63D syndrome

Source : https://www.authorea.com/doi/full/10.22541/au.162066496.69113793

H63D syndrome is a phenotype of a homozygous mutation of the HFE gene H63D, which is otherwise known to cause at most mild classical hemochromatosis. H63D syndrome leads to an iron overload in the body (especially in the brain, heart, liver, skin and