Cleidocranial Dysplasia Latest Advances

Journal: American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics

Published: November 11, 2025

Cleidocranial Dysplasia Latest Advances

Find the Latest Research About Cleidocranial Dysplasia

A Novel 4.2 kb deletion of the 3'UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3'UTR.

A Novel 4.2 kb deletion of the 3'UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3'UTR.

Optimized Approach for Retrieval of Multiple Impacted Teeth in Cleidocranial Dysplasia.

Optimized Approach for Retrieval of Multiple Impacted Teeth in Cleidocranial Dysplasia.

Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variant.

Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variant.

Ossification of the mandible: A regional composite model of intramembranous, parachondral, and endochondral mechanisms.

Ossification of the mandible: A regional composite model of intramembranous, parachondral, and endochondral mechanisms.

Sost deficiency restores calvarial bone thickness without recovery of sutural growth in Runx2 missense mutant mice.

Sost deficiency restores calvarial bone thickness without recovery of sutural growth in Runx2 missense mutant mice.

Early prenatal detection of autosomal dominant skeletal dysplasia using first-trimester ultrasound and cell-free fetal DNA screening: three case reports.

Early prenatal detection of autosomal dominant skeletal dysplasia using first-trimester ultrasound and cell-free fetal DNA screening: three case reports.

Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial Dysplasia.

Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial Dysplasia.

Correlation of RUNX2 Variants With Craniofacial-Dental Phenotypes in Cleidocranial Dysplasia.

Correlation of RUNX2 Variants With Craniofacial-Dental Phenotypes in Cleidocranial Dysplasia.

Branch site mutated mice revealed distinct roles of two Runx2 isoforms in bone development.

Branch site mutated mice revealed distinct roles of two Runx2 isoforms in bone development.

The Impact of Genetics on Craniofacial Dysplasias and Consequent Oral Malformations-Integrative Review.

The Impact of Genetics on Craniofacial Dysplasias and Consequent Oral Malformations-Integrative Review.

Computed Tomography Analysis of Craniofacial Features in Japanese Patients With Cleidocranial Dysplasia.

Computed Tomography Analysis of Craniofacial Features in Japanese Patients With Cleidocranial Dysplasia.

Comment on: "Anatomic assessment of palatal temporary skeletal anchorage devices insertion sites among patients with cleidocranial dysplasia vs controls: A retrospective cone-beam computed tomography analysis".

Comment on: "Anatomic assessment of palatal temporary skeletal anchorage devices insertion sites among patients with cleidocranial dysplasia vs controls: A retrospective cone-beam computed tomography analysis".