Background and Objective: The thalassemic syndromes are geneticaly structural disturbance of Alfa and Beta globin chains. In major Beta-thalassemia the life expectancy depended on frequent blood transfusions that lead to over storage and deposition of Iron in different body-organs (Hemochromatosis) including parathyroid glands, which may cause hupoparathyroidism. This study was done to evaluate the frequency of hypoparathyroidism in thalassemic patients referred to teaching hospitals in Hamedan – Iran. Materials and Methods: This descriptive, cross-sectional study was done on 56 thalassemic patients, which received blood transfusion. Serum Ca , P , PTH , total protein , albumin , Ferritin and BUN cratinine were checked two weeks after last ...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Objective: To determine the status of thyroid function among β-thalassemia major patients dependent ...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
BACKGROUND AND OBJECTIVE: Hypoparathyroidism is one the common complications of endocrine in patient...
Purpose: To determine the prevalence of hypoparathyroidism in transfusion -dependent patients with β...
The present study aimed to determine the prevalence of hypothyroidism, hypoparathyroidism and the fr...
Background: Blood transfusions in thalassemia cases might disturb thyroid gland. Objective: The ob...
Abstract: Objective: The main aim of this study was to find the incidence of hypothyroidism in patie...
Objective: This research's primary objective was to classify the occurrence of hypothyroidism in pat...
Determining the frequency of hypogonadism in thalassemia major patients and clarifying factors affec...
Objective: This research's primary objective was to classify the occurrence of hypothyroidism in pat...
Repeated blood transfusions in thalassemia patients is followed by endocrinopathies as diabetes, hyp...
PubMedID: 29350657Hypoparathyroidism (HPT) is a rare disease with leading symptoms of hypocalcemia, ...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
Objective:Beta thalassemia major is a prevalent hereditary disease in Mediterranean region especiall...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Objective: To determine the status of thyroid function among β-thalassemia major patients dependent ...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
BACKGROUND AND OBJECTIVE: Hypoparathyroidism is one the common complications of endocrine in patient...
Purpose: To determine the prevalence of hypoparathyroidism in transfusion -dependent patients with β...
The present study aimed to determine the prevalence of hypothyroidism, hypoparathyroidism and the fr...
Background: Blood transfusions in thalassemia cases might disturb thyroid gland. Objective: The ob...
Abstract: Objective: The main aim of this study was to find the incidence of hypothyroidism in patie...
Objective: This research's primary objective was to classify the occurrence of hypothyroidism in pat...
Determining the frequency of hypogonadism in thalassemia major patients and clarifying factors affec...
Objective: This research's primary objective was to classify the occurrence of hypothyroidism in pat...
Repeated blood transfusions in thalassemia patients is followed by endocrinopathies as diabetes, hyp...
PubMedID: 29350657Hypoparathyroidism (HPT) is a rare disease with leading symptoms of hypocalcemia, ...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
Objective:Beta thalassemia major is a prevalent hereditary disease in Mediterranean region especiall...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Objective: To determine the status of thyroid function among β-thalassemia major patients dependent ...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...