Browsing by Subject "Thalassemia--Diagnosis"
Now showing items 1-3 of 3
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Comparison of mutation spectrum, hemoglobin profiles and hematological features between transfusion dependent and non-dependent patients of Hb E/β Thalassemia
(Brac University, 2019)Hemoglobin E/β Thalassemia is an inherited anemic genetic disorder that is highly prevalent in the Southern Asia part of the world. Bangladesh falls in the Thalassemia belt of the world. The clinical manifestation of this ... -
Detection of beta globin gene mutations in thalassemia patients in Bangladesh and correlation with hematological parameters
(Brac University, 2018-12)β-thalassemia and hemoglobin E (Hb E) diseases are highly prevalent autosomal recessive disorders characterized by the reduced or absent expression of the β globin gene. β-thalassemia is now regarded as the most common ... -
Mutation patterns in the HBB gene determine the frequency and onset of blood transfusion in patients with beta-thalassemia major and HbE-beta thalassemia
(Brac University, 2019-11)Thalassemia is a blood disorder passed down through families (inherited) in which the body makes an abnormal form or inadequate amount of hemoglobin. Co-inheritance of beta-thalassemia alleles from two parents results ...
