Present chelation protocols have increased the life quality and survival of the patients with β-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 stature (42...
Background: The commonest form of thyroid dysfunction, seen in thalassaemics, is subclinical hypothy...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Objective: This work aims to estimate serum ferritin levels of the B-thalassemia major (BTM) patient...
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 beta-t...
PubMed: 24854890The endocrinological complications in ?-thalassemia major patients do affect the lif...
Aim: Endocrinopathies are common in patients with thalassemia major (TM) and affect their life quali...
Background Endocrine disorders in thalassemia major children patients occur due to iron overload and...
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 Beta thalassemia major (TM) is the most common inherited genetic disorder worldw...
Background: Present transfusion protocols have increased the life expectancy of patients with β-thal...
Thalassemia is a disease of hemolytic anemia characterized by abnormalities in globin chain synthesi...
OBJECTIVE Thalassaemia major is a common and serious medical problem, worldwide. However, there are ...
Endocrine complications in patients with thalassemia major in developing countries may be frequent d...
Background: The commonest form of thyroid dysfunction, seen in thalassaemics, is subclinical hypothy...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Objective: This work aims to estimate serum ferritin levels of the B-thalassemia major (BTM) patient...
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 beta-t...
PubMed: 24854890The endocrinological complications in ?-thalassemia major patients do affect the lif...
Aim: Endocrinopathies are common in patients with thalassemia major (TM) and affect their life quali...
Background Endocrine disorders in thalassemia major children patients occur due to iron overload and...
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 Beta thalassemia major (TM) is the most common inherited genetic disorder worldw...
Background: Present transfusion protocols have increased the life expectancy of patients with β-thal...
Thalassemia is a disease of hemolytic anemia characterized by abnormalities in globin chain synthesi...
OBJECTIVE Thalassaemia major is a common and serious medical problem, worldwide. However, there are ...
Endocrine complications in patients with thalassemia major in developing countries may be frequent d...
Background: The commonest form of thyroid dysfunction, seen in thalassaemics, is subclinical hypothy...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Objective: This work aims to estimate serum ferritin levels of the B-thalassemia major (BTM) patient...