Abstract

Thalassemia is the most common genetic blood disease in the world and varies in different population group in the world. In thalassemic patients liver damage is augmented when age of the patients are increase. These are due to increasing age with advancement of disease progression, repeated blood transfusion, less use/ intolerance of iron chelating agent, decreased activity of hepatocyte to rescue them in such excess billirubin and iron flood. Secondary to hypersplenism. Iron overload due to frequent transfusions in ?-thalassemia results in abnormal organ function tests. Proper and timely screening of these parameters can help in early diagnosis & prevention of iron overload. Iron overload is a main leading cause of elevated liver enzymes, and presence of HCV infection is significantly related to the increased iron overload14. Liver injury whether acute or chronic, eventually results in an increase in serum concentrations of Alanine transaminase (ALT) and Aspartate transaminase (AST). In transfusion dependent thalassemia patients iron overload is often inevitable and exposed to transfusion associated infections. Apart from these when the age is more, the disease progresses with their complication like hepatic injury. The thalassemia patient develops liver fibrosis as a result of iron overload due to excessive blood transfusion and also from excess intestinal absorption. N Sultana et al.6 showed that serum ferritin and serum bilirubin parameter of iron over load and jaundice are correlated.

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