Background: The commonest form of thyroid dysfunction, seen in thalassaemics, is subclinical hypothyroidism due to abnormalities of the thyroid gland which, leads to insufficient production of thyroid hormones. However, the frequency of hypothyroidism varies depending on the region, quality of management and treatment protocols. Aim: This study was conducted with the aim of investigating the frequency of hypothyroidism in children with beta-thalassemia major and to study its correlation with serum ferritin. Material and methods: A case-control study was carried out in the OPD, Medical College, Kolkata. It included 100 children with Beta–Thalassemia major as cases. Hundred age and gender matched healthy controls were also included in the stu...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
Background: Blood transfusions in thalassemia cases might disturb thyroid gland. Objective: The ob...
Introduction: Thalassemia is a genetic condition and is one of the commonest single-gene hereditary ...
Background. Thalassemia is the most common genetic disorder worldwide. Use of iron chelators has imp...
Objective: Hypothyroidism usually appears in the second decade of life and is thought to be associa...
Background Endocrine disorders in thalassemia major children patients occur due to iron overload and...
Objective: to find correlation between serum ferritin and thyroid stimulating hormones among thalass...
Objective: to find correlation between serum ferritin and thyroid stimulating hormones among thalass...
Background Severe iron overload due to recurrent transfusions for chronic anemia and inadequate iron...
Objective: The main aim of this research work is to compare the mean serum iron-containing protein k...
Basal thyroid function was assessed by serum thyroxine, tri-iodothyronine and thyroid-stimulating ho...
Background: Thyroid hormones are required for normal development as well as regulating metabolism in...
Objective: Despite regular transfusions and iron-chelation therapies, endocrine complications still ...
Background and Aim: Iron deficiency is one of the most common nutritional disorders in the world, an...
Introduction: Thyroid gland is a bi-lobed endocrine gland and it secretes thyroxin (T4) and tri-iodo...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
Background: Blood transfusions in thalassemia cases might disturb thyroid gland. Objective: The ob...
Introduction: Thalassemia is a genetic condition and is one of the commonest single-gene hereditary ...
Background. Thalassemia is the most common genetic disorder worldwide. Use of iron chelators has imp...
Objective: Hypothyroidism usually appears in the second decade of life and is thought to be associa...
Background Endocrine disorders in thalassemia major children patients occur due to iron overload and...
Objective: to find correlation between serum ferritin and thyroid stimulating hormones among thalass...
Objective: to find correlation between serum ferritin and thyroid stimulating hormones among thalass...
Background Severe iron overload due to recurrent transfusions for chronic anemia and inadequate iron...
Objective: The main aim of this research work is to compare the mean serum iron-containing protein k...
Basal thyroid function was assessed by serum thyroxine, tri-iodothyronine and thyroid-stimulating ho...
Background: Thyroid hormones are required for normal development as well as regulating metabolism in...
Objective: Despite regular transfusions and iron-chelation therapies, endocrine complications still ...
Background and Aim: Iron deficiency is one of the most common nutritional disorders in the world, an...
Introduction: Thyroid gland is a bi-lobed endocrine gland and it secretes thyroxin (T4) and tri-iodo...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
Background: Blood transfusions in thalassemia cases might disturb thyroid gland. Objective: The ob...
Introduction: Thalassemia is a genetic condition and is one of the commonest single-gene hereditary ...