The tissue-resident skeletal stem cells (SSCs), which are self-renewal and multipotent,
continuously provide cells (including chondrocytes, bone cells, marrow adipocytes, and …

Cleidocranial dysplasia (CCD) spectrum disorder is a skeletal dysplasia that represents a
clinical continuum ranging from classic CCD (triad of delayed closure of the cranial sutures …

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

Cleidocranial dysplasia (CCD) is a rare autosomal dominant disorder caused by mutations
in the Runx2 gene. The CCD is characterized by frontal bossing, a patent anterior fontanelle …

Oligodontia is a developmental dental anomaly defined by the absence of 6 or more
permanent teeth, excluding the third molars. We performed a review with a systematic …

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 …

Patients with cleidocranial dysplasia (CCD) caused by mutations in RUNX2 have severe
dental anomalies, including delayed or absent eruption of permanent teeth. This requires …

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 skeletal dysplasia caused by
runt-related transcription factor 2 (RUNX2) mutations. In addition to the regular missense …

Purpose This study aimed to investigate the panoramic imaging features of cleidocranial
dysplasia (CCD) with a relatively large sample. Materials and Methods The panoramic …