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Screening of liver disease in children with transfusion dependent thalassemia at Minia University Hospitals
References:
10
Abstract
Background: Beta thalassemia is a hereditary disorder that results from genetic mutations in the synthesis of beta-globin chains.The imbalance of globin chain synthesis results in aggregates that damage red cell membranes, resulting in intravascular hemolysis.This results in chronic anemia which causes erythroid hyperplasia and extramedullary hematopoiesis."TDT" patients are liable for several med...
Keywords
Sustainable Development Goals (SDG)
2022
Article
Open Access
2-Y Citation Average
0.16
Language
Country
Screening of liver disease in children with transfusion dependent thalassemia at Minia University Hospitals
References:
10
Abstract
Background: Beta thalassemia is a hereditary disorder that results from genetic mutations in the synthesis of beta-globin chains.The imbalance of globin chain synthesis results in aggregates that damage red cell membranes, resulting in intravascular hemolysis.This results in chronic anemia which causes erythroid hyperplasia and extramedullary hematopoiesis."TDT" patients are liable for several med...
Keywords
Sustainable Development Goals (SDG)
2022
Article
Open Access
2-Y Citation Average
0.16
Language
Country