Objective: Beta Thalassemia (βT) patients present a unique facial appearance and specific
craniofacial, jaw and dental patterns. Although this anomaly often requires orthodontic …

Rapid blood cell turnover and bone marrow expansion caused by beta-thalassemia (βT)
result in craniofacial and dentoalveolar anomalies. This report presents a systematic review …

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 …

Aim: The aim of this report is to present the management of the maxillary deformity and
subsequent implant therapy of a case with β-thalassemia major. Background: β-thalassemia …

Background Thalassemia is a group of congenital disorders which is characterized by a
deficient synthesis of alfa or beta globulin chains in hemoglobin molecules. Due to the …

Aim: To investigate cephalometric craniofacial parameters (skeletal and dental) of β‐
thalassemic‐major patients and to compare findings with a group of healthy patients in the …

Patients suffering from hemoglobinopathies may suffer from pathogic dental and orofacial
features. This study aimed to assess the prevalence of malocclusion and the need for …

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

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 …

Objective: To evaluate the prevalence and severity of malocclusion in children suffering from
β-thalassemia and to assess orthodontic treatment need using Grainger's Treatment Priority …