BACKGROUND Hypertriglyceridemia thalassemia syndrome is a rare condition that occurs in patients with thalassemia.It typically presents with a combination of profound anemia and milky serum.Although previous case seri...
BACKGROUND Iron overload cardiomyopathy is a significant cause of morbidity and mortality in transfusion-dependent thalassemia patients.Standard iron chelation therapy is less efficient in alleviating iron accumulatio...
Objective:Our study aimed to investigate the ototoxicity associated with the iron chelator deferasirox in patients withβ-thalassemia major,who were receiving regular transfusion therapy,along with evaluating the data...
Objective: To analyze trends in prevalence, mortality, and disability-adjusted life years (DALYs) of childhood thalassemia from 1990 to 2021. Methods: Using the 2021 Global Burden of Disease (GBD) database, we conduct...
Introduction: Sickle cell disease and thalassemia are the most frequent hemoglobinopathies. During their evolution, they present certain complications, among which are two neurosurgical emergencies, namely spontaneous...
Background:Thalassemia is a prevalent condition characterized by decreased production or absence of hemoglobin globin chains.There are 2 types of thalassemia,alpha thalassemia and beta thalassemia(β-thalassemia),clas...
Mediterranean anemia is a genetic disease that currently relies heavily on expert clinical experience to determine whether patients are affected. This method is overly reliant on expert experience and is not precise e...
supported by the National Key R&D Program ofChina(No.2019YFA0109900,2019YFA0109901,2019YFA0802800,2019YFA0110803,2021YFC2700901);the Shanghai Municipal Commission for Science and Technology(No.19PJ1403500);the National Natural Science Foundation of China(No.82101802,81300383);the Scientific Research of BSKY(No.XJ2020025)from Anhui Medical University,and the Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences(No.2019PT310002);Young Taishan Scholar Foundation of Shandong Province,China(No.tsqn202103167);Clinical Research Center of Shandong University(China)(No.2020SDUCRCC015).
Genetic mutations cause aberrant splicing,one of the important molecular mechanisms in human diseases.Ivs2-654,a mutation causing aberrant splicing ofβ-globin premRNA and contributing toβ-globin deficiency,is one of...
Introduction: Thalassemia disorder is a genetic disease that causes the blood to have less hemoglobin than normal, the main requirement to control thalassemia’s propagation is to educate the entire society. Methodolo...
Iron overload is a condition involving excessive iron deposit in various organs,the liver being the main target organ for iron deposition and overload which are associated with significant liver morbidity and mortalit...