Tooth number abnormality is one of the most common dental developmental diseases,
which includes both tooth agenesis and supernumerary teeth. Tooth development is …

Coronoid process hyperplasia (CPH) is an oral and maxillofacial surgical disease that can
result in restricted jaw movement due to an enlarged and elongated mandibular coronoid …

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 …

Background Cleidocranial dysplasia (CCD) is an autosomal dominant hereditary disorder.
Besides skeletal abnormalities, CCD is often associated with dental complications, such as …

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 …

Objectives: Cleidocranial dysplasia (CCD) is a rare skeletal syndrome affecting craniofacial
and dental development. As a consequence, conventional cephalometric landmarks may …

Objective Hypoplasia of the medial pterygoid process of the sphenoid bone is a distinct
skeletal phenotype in runt-related transcription factor 2 (Runx2) heterozygous mice and …

Background: Cleidocranial dysostosis (CCD) is a rare genetic disease that compromises
normal bone development, caused by the alteration in the RUNX2 gene of chromosome 6p …

Background This retrospective study aims to evaluate the relative representation of
individual types of developmental odontogenic cysts (DOCs), especially from the …

Cleidocranial dysplasia is a rare autosomal dominant disorder. It is mainly characterized by
hypoplastic clavicles, delayed fontanelle closure, and a large foramen magnum with dental …