Present chelation protocols have increased the life quality and survival of the patients with beta-thalassemia major (BTM). However, endocrine complications are still mostly experienced. The aim of this study was to determine the prevalence of endocrine complications in children with BTM, and to study the relationship between serum ferritin levels and complications. Forty-five children (female: 23/male: 22, mean age: 12.39 +/- 3.72 y) with BTM were enrolled into the study. Blood samples were taken after an overnight fasting, early in the morning from entire study group. Median (range) serum ferritin of the patients was 1365 ng/mL (362 to 5996 ng/mL). The most prevalent endocrine complications were vitamin D insufficiency (54.5%), short stat...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
WOS: 000174189100011PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studie...
Introduction: Beta-thalassemia major patients frequently have endocrine and metabolic disorders. As ...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
PubMed: 24854890The endocrinological complications in ?-thalassemia major patients do affect the lif...
Objective: Despite regular transfusions and iron-chelation therapies, endocrine complications still ...
Background: This study aimed to estimate the prevalence of complications and in β-thalassemia patien...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Background Endocrine disorders in thalassemia major children patients occur due to iron overload and...
Background: Present transfusion protocols have increased the life expectancy of patients with β-thal...
Objective: This work aims to estimate serum ferritin levels of the B-thalassemia major (BTM) patient...
Background: The commonest form of thyroid dysfunction, seen in thalassaemics, is subclinical hypothy...
Introduction: Thalassemia is a genetic condition and is one of the commonest single-gene hereditary ...
Abstract Background Beta thalassemia major (TM) is the most common inherited genetic disorder worldw...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
WOS: 000174189100011PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studie...
Introduction: Beta-thalassemia major patients frequently have endocrine and metabolic disorders. As ...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
PubMed: 24854890The endocrinological complications in ?-thalassemia major patients do affect the lif...
Objective: Despite regular transfusions and iron-chelation therapies, endocrine complications still ...
Background: This study aimed to estimate the prevalence of complications and in β-thalassemia patien...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Background Endocrine disorders in thalassemia major children patients occur due to iron overload and...
Background: Present transfusion protocols have increased the life expectancy of patients with β-thal...
Objective: This work aims to estimate serum ferritin levels of the B-thalassemia major (BTM) patient...
Background: The commonest form of thyroid dysfunction, seen in thalassaemics, is subclinical hypothy...
Introduction: Thalassemia is a genetic condition and is one of the commonest single-gene hereditary ...
Abstract Background Beta thalassemia major (TM) is the most common inherited genetic disorder worldw...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
WOS: 000174189100011PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studie...
Introduction: Beta-thalassemia major patients frequently have endocrine and metabolic disorders. As ...