Vr. Gordeuk et al., ETIOLOGIES, CONSEQUENCES, AND TREATMENT OF IRON OVERLOAD, Critical reviews in clinical laboratory sciences, 31(2), 1994, pp. 89-133
From a global perspective, severe systemic iron overload occurs predom
inantly in individuals affected by geographically specific genetic mut
ations that permit the daily absorption from the diet of more iron tha
n is physiologically needed. Two main types of hereditary iron overloa
d are well. recognized: (1) HLA-linked hemochromatosis in populations
derived from Europe and (2) iron overload complicating thalassaemia ma
jor and intermedia syndromes in Southeast Asia, the Middle East, and t
he Mediterranean. Another very common form of iron overload occurs in
Africa and is clearly related to high dietary iron content; recent evi
dence suggests that a genetic predisposition may also contribute to th
e pathogenesis. Patients with iron overload may develop multiorgan sys
tem toxicity; aggressive therapy with phlebotomy or iron chelation to
remove excess iron from the body prevents organ damage and prolongs li
fe.