A Compound Heterozygous of Hb E and Beta Thalassemia Independent of Transfusion: A Rare Case Report
نویسندگان
1 Departments of Pathology, University College of Medical Sciences & GTB hospital, Delhi - Departments of Pathology, University College of Medical Sciences & GTB hospital, Delhi
2 Departments of Pathology, University College of Medical Sciences & GTB hospital, Delhi - Departments of Pathology, University College of Medical Sciences & GTB hospital, Delhi
3 Departments of Pathology, University College of Medical Sciences & GTB hospital, Delhi - Departments of Pathology, University College of Medical Sciences & GTB hospital, Delhi
doi
10.18502/ijpho.v14i4.16605چکیده
Hemoglobinopathy is now a worldwide problem. Mainly described in Southeast Asian countries. A compound heterozygous form of hemoglobin (Hb) E & β thalassemia was reported to be 50% of all severe forms of thalassemia. Clinical presentation of HbE/ b thalassemia is reported to be moderate to severe anemia. The children usually present at the ...
