Advances in treatment of thalassemia have led to the aging of thalassemic patients, and
consequently concern about successful reproductive outcome is augmented. Although …

Bone disorders in patients with thalassemia major (TM) and intermedia (TI) constitute
complex conditions that result from various factors affecting the growing skeleton. Although …

Beta-thalassemia and particularly its transfusion-dependent form (TDT) is a demanding
clinical condition, requiring life-long care and follow-up, ideally in specialized centers and by …

OBJECTIVE We systematically explored the link of pancreatic iron with glucose metabolism
and with cardiac complications in a cohort of 1,079 patients with thalassemia major (TM) …

Anemia in childhood is defined as a hemoglobin (Hb) concentration below cut off levels
established by the World Health Organization:< 11 g/dl in children aged 6–59 months,< 11.5 …

Abstract Background and Aims One of the most common hemoglobinopathies globally
related to blood transfusion and iron overload in the body is thalassemia syndrome …

Objective The aim of our study was to evaluate the prevalence of endocrinopathies and liver
dysfunction, in relation to LIC and serum ferritin level, in a selected group of adolescents and …

Thalassemia and sickle cell disease (SCD) are disorders of hemoglobin that affect millions
of people worldwide. The carrier states for these diseases arose as common, balanced …

Anaemia is a global public health problem affecting both developing and developed
countries with major consequences for human health as well as social and economic …

Abstract Changes in thyroid function and thyroid function tests occur in patients with β-
thalassemia major (TM). The frequency of hypothyroidism in TM patients ranges from 4% to …