Osteoporosis represents an important cause of morbidity in adult patients with thalassaemia
major (TM). The pathogenesis of osteoporosis in TM is multifactorial, and includes bone …

Increased survival in patients with β thalassemia major (TM) allowed for several
complications of the disease and its treatment to manifest, one of which is bone disease …

Thalassemia bone disease is a common and severe complication of thalassemia—an
inherited blood disorder due to mutations in the α or β hemoglobin gene. In its more severe …

Objective This study aimed to evaluate the radiomorphometric indexes and fractal
dimension (FD) on dental panoramic radiography (DPR) of Thalassemia Major (TM) …

In addition to the severe beta thalassemias, hematologists have begun to recognize the
more severe forms of alpha thalassemia, namely hemoglobin (Hb) H disease and Hb H/Hb …

The Task Force focusing on the use of dual energy X-ray absorptiometry (DXA) in children
and adolescents with diseases that may affect the skeleton reviewed over 300 articles to …

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

Thalassemia-associated osteoporosis constitutes a major complication in patients with
thalassemia. This review presents the existing studies on the treatment of thalassemia …

Osteoporosis in beta‐thalassaemia is multifactorial; increased osteoclast function seems to
play an important role in its pathogenesis. The aim of this study was to evaluate the effect of …

Osteoporosis represents a prominent cause of morbidity in patients with thalassemia. The
delay in sexual maturation, the presence of diabetes and hypothyroidism, the parathyroid …