الفهرس | Only 14 pages are availabe for public view |
Abstract This work included 30 patients, 15 males and 15 females. Their age varied from 2 to 15 years. They included 1’6 patients with hemoglobinopathies (13 with beta-thalassemia, 2 with sickle cell anemia and one patient with sickle cell thalassemia), 6 with idiopathic thrombocytopenic purpura, 4 with idiopathic hypersplenism, 3 with autoimmune hemolytic anemia and one patient with hereditary spherocytosis.The patients in each group were subjected to full history taking, thorough clinical examination and the required investigations. |