Background: Cleidocranial dysplasia (CCD) is a rare, autosomal dominant skeletal
dysplasia with a prevalence of one per million births. The main causes of CCD are mutations …

Introduction Cleidocranial dysplasia (CCD) is a rare disease characterized by craniofacial,
skeletal, and oral anomalies. The disease prevalence is estimated to be 1 per million …

Background and aim Cleidocranial dysplasia is a rare disorder of skeletal development that
mainly promotes, among other malformations, inadequate development of clavicles and …

Cleidocranial dysplasia (CCD) is a rare autosomal dominant disorder with facial, dental, and
skeletal impairments. Affected individuals have varying degrees of skull, shoulder, dental …

Background Cleidocranial dysplasia (CCD) is a rare and underdiagnosed congenital
disorder in dentistry. The purpose of this study was to illustrate and quantify the maxillofacial …

Cleidocranial dysplasia (CCD; OMIM 119600) is a rare autosomal dominant skeletal
dysplasia, which is mainly characterized by persistently open or delayed closure of …

Cleidocranial dysplasia is a rare disease with an autosomal‐dominant inheritance that
mainly affects the bones of the axial skeleton. In this report, we discuss the clinical and …

Cleidocranial dysplasia (CCD) is a rare genetic condition that affects the bones and teeth. In
our study, we presented three cases of CCD, including one with a new mutation and two …

Cranial sutures are complex structures integrating mechanical forces with osteogenesis
which are often affected in craniofacial syndromes. While premature fusion is frequently …

Anterior openbite (AOB) malocclusion has been regarded as a complex and challenging
malocclusion to manage regarding diagnostic and treatment decisions. The aetiology of …