Different Types of Complications in Patients Suffering from B-Thalassemia (Thalassemia Major)
نویسندگان
چکیده
منابع مشابه
Quality of Life in Patients Suffering from Beta-Thalassemia Major in Amirkola, Iran
Abstract Introduction: Thalassemia is regarded as a genetic hematologic disease that affects various aspects of patients’ life. Measuring the health-related quality of life is a multidimensional concept that focuses on the disease as well as its treatment. Materials and methods: This cross-sectional study consisted of 50 adolescents aged 12-18 years suffering from Thalassemia major, ou...
متن کاملA study of peripheral blood neutrophils’ function in patients suffering from thalassemia major
Background: Thalassemia is the most common blood disorder in the world. This hereditary anemia, Which develops due to a constitutional imbalance in alpha and beta chains of adult haemoglobin (hbA), has serious and life- threatening complications (accompanied by haemolysis and bone deformities) in its major form. We may encounter a diverse collection of articles in world research centers about t...
متن کاملNeurological complications in b-thalassemia
Over the years, several reports have demonstrated involvement of the nervous system in b-thalassemia patients. Neurological complications have been attributed to various factors such as chronic hypoxia, bone marrow expansion, iron overload, and desferrioxamine neurotoxicity. In most cases, neurological involvement does not initially present with relevant signs or symptoms (i.e., is subclinical)...
متن کاملDiabetes mellitus and cardiac complications in thalassemia major patients
Background The relationship between diabetes mellitus (DM) and cardiac complications has never been systematically studied in thalassemia major (TM). The aim of this crosssectional study was to evaluate in a large historical cohort of TM in the cardiovascular magnetic resonance (CMR) era if DM was associated with an higher prevalence and risk of heart complications, also regardless to the prese...
متن کاملEndocrinopathies in Thalassemia major patients in Thalassemia Center Jakarta, Indonesia
Background Regular transfusion in thalassemia major patients increases life expectancy and improves quality of life, but results in iron overload, which had toxic effects to organs including endocrine glands. The introduction of iron chelation therapy has reduced its toxicity, but complications may still occur. In Indonesia, most of our patients did not receive optimal iron chelation therapy, w...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of Gandhara Medical and Dental Science
سال: 2017
ISSN: 2618-1452,2312-9433
DOI: 10.37762/jgmds.4-1.30