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Abstract
Thalssemia intermedia is clinical form of β –
thalassemia in which the clinical manifestation is
less sever than thalassemia major. We studied 58
patients who were diagnosed as thalassemia
intermedia and who are attending the hematology
clinic of Cairo University Children Hospital. We
studied their personal data, such as : age , sex,
residence and consangunity, clinical criteria as age
at onest of the disease, complaint , presence of
pallor, juandice and hemolytic facies, requirements
to transfusion therapy as well as the initial diagnostic
values such as CBC and HB electrophoresis