The relationship between face and disease has been discussed from thousands years ago,
which leads to the occurrence of facial diagnosis. The objective here is to explore the …

The aim of this paper is to review the literature and identify orofacial manifestations of
hematological diseases, with particular reference to anemias and disorders of hemostasis. A …

The skeletal changes of untreated thalassaemia result from ineffective erythropoiesis and
expansion of the bone marrow and affect every part of the skeleton. These changes include …

Objective: To assess the prevalence of periodontal disease, orofacial changes and
craniofacial abnormalities in patients with thalassemia major (TM). Dental management is …

Facial phenotypes are extensively studied in medical and biological research, serving as
critical markers that potentially indicate underlying genetic traits or medical conditions. With …

Background The objective of this study is to evaluate the prevalence of malocclusion and
treatment needs in transfusion dependent β-thalassemia major children. Methods One …

Background: β-thalassaemia major is a hereditary hemolytic anemia and the patients often
experience growth retardation, protrusive maxilla, and depressed nasal bride leading to …

Objectives: This investigation aimed to compare the radiographic changes and root and
crown-body lengths of the mandibular first permanent molar in a group of thalassaemic …

Structured abstract Authors–Amini F, Jafari A, Eslamian L, Sharifzadeh S Objective–To study
cephalometric and facial features of Iranian children with beta‐thalassemia major. Design …

Objective: Thalassemias major are the most common autosomal recessive disorders; they
are characterized by anomalies in the synthesis of the beta chains of hemoglobin and are …