RESUMEN
Enhanced years of survival have led to the unmasking of management related complications with the recognition of the existence of a chronic hypercoagulable state in thalassemic patients. This study aims at determining the levels of the three main antithrombophilic factors namely protein C, protein S and antithrombin III in Egyptian children with beta thalassemia major. Sixty children with beta thalassemia major with a mean age of 12.2 +/- 1.88 years and male: female ratio 1.7: 1 were enrolled in the study. They were subjected to history taking, clinical examination and laboratory investigations including levels of ferritin by IRMA, protein C, protein S, and antithromobin III by ELISA. Protein C was deficient in 16 [26.7%] of cases, protein S was deficient in 8 [13.3%] of cases while none had deficiency of antithrombin III. None of our cases had a history of thromboembolic events. These abnormalities were not related to the state of HCV infection or to the type of chelation whether oral or subcutaneous. Protein C deficiency was present more in older patients. Abnormalities in protein C, protein S are frequently observed even without manifesting hypercoagulable states in our studied thalassemia major children