Thalassemia syndromes are complex systemic disorders. Clinical complications are related
to the underlying pathophysiological mechanisms, namely ineffective erythropoiesis, chronic …

Background: Thalassemia is categorized based on the abnormal globin chain and is divided
into primary, intermediate, and minor subtypes based on the chain abnormality, respectively …

Background and objectives: Sickle cell disease and sickle?-thalassemia are hemolytic
diseases characterized by chronic destruction of the abnormal red cells with consequent …

Conclusão: A abordagem do doente pediátrico com litíase vesicular assintomática
permanece um tema controverso, sendo necessários mais estudos que caracterizem esta …

مقدمه با توجه به گزارشهایی مبنیبر وجود سنگهای صفراوی در بیماران تالاسمی و شیوع این
بیماری در مازندران، این مطالعه با هدف بررسی نیاز به کلهسیستکتومی همزمان در بیماران مبتلا به …‎

Background: Cholelithiasis, while infrequently found in children, carries a significant risk for
those with underlying conditions like thalassemia compared to the general population. This …

Kolestasis dapat disebabkan oleh gangguan fungsional hepatosit dalam sekresi empedu
dan/atau karena obstruksi pada setiap tingkat jalur ekskresi empedu. Pada pasien …

Background: Thalassemias are inherited blood disorders, characterized by ineffective
erythropoiesis. Incidence of thalassemia syndromes is high in South Asia including India …

Introduction: This study aims to investigate the necessity of simultaneous cholecystectomy in
thalassemia major patients undergoing splenectomy, in light of reports regarding the …

HbE/β-thalassaemia is the most common form of βthalassaemia. The clinical presentation of
HbE thalassaemia is heterogeneous, symptomatic individuals may vary significantly, while …