Determining the frequency of hypogonadism in thalassemia major patients and clarifying factors affecting it can be helpful in reducing related complications and improving the prognosis. The objective of the present study was to establish the frequency of hypogonadism in thalassemia major patients of Hazrat-e Rasool Akram Hospital during 2013-2017. A descriptive and analytic cross-sectional observation was carried out for this study and 285 thalassemia major patients were selected via convenience sampling. The frequency of hypogonadism among samples was assessed and the relationship between hypogonadism and different factors was analyzed. One hundred forty-six patients (51/2) had hypogonadism. A statistically significant relationship was fou...
Background: Multi-transfused thalassemia major (TM) patients frequently develop severe endocrine com...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studied to determine the e...
Background and aims: Hypogonadism is one of the most common endocrine complications in patients with...
Objective: To determine the prevalence and risk factors of hypogonadotropic hypogonadism in transfus...
Background: Present transfusion protocols have increased the life expectancy of patients with β-thal...
AbstractDespite recent advances in iron chelation therapy, excess iron deposition in pituitary gonad...
BACKGROUND AND OBJECTIVE: Hypoparathyroidism is one the common complications of endocrine in patient...
Background and Objective: The thalassemic syndromes are geneticaly structural disturbance of Alfa an...
Introduction: Thalassemia Major Illness is mainly created as a progressive hemolytic anemia within t...
AIM: The type of malocclusion most often seen in beta thalassemic patients is represented by Angl...
Abstract: Objective: The main aim of this study was to find the incidence of hypothyroidism in patie...
OBJECTIVE Thalassaemia major is a common and serious medical problem, worldwide. However, there are ...
Abstract. Introduction. In males, acquired hypogonadotropic hypogonadism (AHH) includes all disorder...
Growth disorders are considered as one of the common complications of thalassemia major patients. Th...
Background: Multi-transfused thalassemia major (TM) patients frequently develop severe endocrine com...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studied to determine the e...
Background and aims: Hypogonadism is one of the most common endocrine complications in patients with...
Objective: To determine the prevalence and risk factors of hypogonadotropic hypogonadism in transfus...
Background: Present transfusion protocols have increased the life expectancy of patients with β-thal...
AbstractDespite recent advances in iron chelation therapy, excess iron deposition in pituitary gonad...
BACKGROUND AND OBJECTIVE: Hypoparathyroidism is one the common complications of endocrine in patient...
Background and Objective: The thalassemic syndromes are geneticaly structural disturbance of Alfa an...
Introduction: Thalassemia Major Illness is mainly created as a progressive hemolytic anemia within t...
AIM: The type of malocclusion most often seen in beta thalassemic patients is represented by Angl...
Abstract: Objective: The main aim of this study was to find the incidence of hypothyroidism in patie...
OBJECTIVE Thalassaemia major is a common and serious medical problem, worldwide. However, there are ...
Abstract. Introduction. In males, acquired hypogonadotropic hypogonadism (AHH) includes all disorder...
Growth disorders are considered as one of the common complications of thalassemia major patients. Th...
Background: Multi-transfused thalassemia major (TM) patients frequently develop severe endocrine com...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studied to determine the e...