Background Cleidocranial dysplasia (CCD) is a genetic disorder with an autosomal
dominant inheritance pattern. CCD characterized by abnormal clavicles, patent sutures 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 …

Oral Diseases (2012) 18, 184–190 Background: Cleidocranial dysplasia (CCD) is a
dominantly inherited autosomal disease characterized by typical bone defects including …

Cleidocranial dysplasia (CCD) is an autosomal-dominant malformation syndrome affecting
bones and teeth. The most common skeletal and dental abnormalities in affected individuals …

Abstract Cleidocranial dysplasia (CCD, MIM 119600) is a rare autosomal dominant disorder
affecting bone, cartilage, craniofacial growth, and tooth formation leading to supernumerary …

Cleidocranial Dysplasia: A Review of Clinical, Radiological,... : Journal of Craniofacial Surgery
Cleidocranial Dysplasia: A Review of Clinical, Radiological, Genetic Implications and a …

Cleidocranial dysplasia (CCD) is a rare congenital defect of autosomal dominant
inheritance, primarily affecting bones that undergo intra‐membranous ossification. Herein is …

BACKGROUND Cleidocranial dysplasia (CCD) is an autosomal‐dominant skeletal
dysplasia syndrome that is characterized by widely patent calvarial sutures, clavicular …

Disease characteristics. Cleidocranial dysplasia (designated as CCD in this GeneReview) is
a skeletal dysplasia characterized by delayed closure of the cranial sutures, hypoplastic or …

Cleidocranial dysplasia (CCD) is a skeletal disorder affecting cranial sutures, teeth, and
clavicles, and is associated with the RUNX2 mutations. Although numerous patients have …