INTRODUCTION: Beta Thalassemia are group of inherited disorder of haemoglobin synthesis caused by genetic mutations that reduce or prevent the synthesis of beta globin chain of haemoglobin. These patient requires regular blood transfusion therapy to overcome the effects of anemia leading to iron overload in the body tissues causing morbidity and mortality in these patient and hence it is essential to monitor the iron overload in these patients. AIM OF THE STUDY: To correlate iron overload in oral exfoliative buccal cells with serum ferritin level among Beta Thalassemia Major patient. MATERIALS AND METHOD: With the study group of 50 beta thalassemia patients with the control groups of 50 healthy subject their buccal squamous cells have...
Beta- thalassemia major is a type of inherited blood disorder, characterized by impaired synthesis...
Thalassemia is a hereditary disorder characterised by changes in organ function and iron overload re...
Beta-thalassemia major is a genetic disorder adversely affecting the life of the patient and the who...
Introduction: Thalassemia is a genetic condition and is one of the commonest single-gene hereditary ...
INTRODUCTION: Beta-thalassemias are a group of hereditary blood disorders characterized by absence o...
Thalassemia is a group of genetically inherited disorder of hemoglobin characterized by reduced synt...
Introduction: Iron overload is the main cause of morbidity and mortality in patients with β-tha...
Introduction: The feature of beta-thalassemia (β-TT) is common in this subcontinent as well as in Pa...
Introduction: Thalassemia is the most common genetic disorder all over the world as per WHO and so p...
Background: HFE gene mutations have been shown to be responsible for hereditaryhemochromatosis. Thei...
Objective: To identify the co-existence of iron deficiency and iron overload in individuals with bet...
Background: Thalassemia is a major health problem in developing and developed countries and suffers ...
Background: Thalassemia is a genetic disease having 3-7% carrier rate in Indians. It is transfusion...
Objective: To evaluate causes of hospitalization (due to complications of iron overload and other ca...
Introduction: Regular blood transfusion for β-thalassemia patients is a life-saving therapy, hence, ...
Beta- thalassemia major is a type of inherited blood disorder, characterized by impaired synthesis...
Thalassemia is a hereditary disorder characterised by changes in organ function and iron overload re...
Beta-thalassemia major is a genetic disorder adversely affecting the life of the patient and the who...
Introduction: Thalassemia is a genetic condition and is one of the commonest single-gene hereditary ...
INTRODUCTION: Beta-thalassemias are a group of hereditary blood disorders characterized by absence o...
Thalassemia is a group of genetically inherited disorder of hemoglobin characterized by reduced synt...
Introduction: Iron overload is the main cause of morbidity and mortality in patients with β-tha...
Introduction: The feature of beta-thalassemia (β-TT) is common in this subcontinent as well as in Pa...
Introduction: Thalassemia is the most common genetic disorder all over the world as per WHO and so p...
Background: HFE gene mutations have been shown to be responsible for hereditaryhemochromatosis. Thei...
Objective: To identify the co-existence of iron deficiency and iron overload in individuals with bet...
Background: Thalassemia is a major health problem in developing and developed countries and suffers ...
Background: Thalassemia is a genetic disease having 3-7% carrier rate in Indians. It is transfusion...
Objective: To evaluate causes of hospitalization (due to complications of iron overload and other ca...
Introduction: Regular blood transfusion for β-thalassemia patients is a life-saving therapy, hence, ...
Beta- thalassemia major is a type of inherited blood disorder, characterized by impaired synthesis...
Thalassemia is a hereditary disorder characterised by changes in organ function and iron overload re...
Beta-thalassemia major is a genetic disorder adversely affecting the life of the patient and the who...