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Metabolomics profiling of cleidocranial dysplasia

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0 Published in 2018 at "Clinical Oral Investigations"

DOI: 10.1007/s00784-018-2496-9

Abstract: ObjectivesCleidocranial dysplasia (CCD) is a rare autosomal-dominantly inherited skeletal dysplasia that is predominantly associated with heterozygous mutations of RUNX2. However, no information is available regarding metabolic changes associated with CCD at present.Materials and methodsWe analyzed… read more here.

Keywords: ccd; profiling cleidocranial; metabolomics profiling; dysplasia ... See more keywords

An overview of the intraoral features and craniofacial morphology of growing and adult Japanese cleidocranial dysplasia subjects.

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1 Published in 2022 at "European journal of orthodontics"

DOI: 10.1093/ejo/cjac039

Abstract: BACKGROUND Orthodontic treatment for cleidocranial dysplasia (CCD) requires an understanding of the nature of the retained deciduous teeth, supernumerary teeth, delayed eruption of the permanent teeth, and craniofacial morphology from childhood to adulthood. This study… read more here.

Keywords: cleidocranial dysplasia; supernumerary teeth; craniofacial morphology; adult japanese ... See more keywords

Amyloid-mediated remineralization for tooth hypoplasia of cleidocranial dysplasia

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2 Published in 2023 at "Frontiers in Cellular and Infection Microbiology"

DOI: 10.3389/fcimb.2023.1143235

Abstract: Introduction Cleidocranial dysplasia (CCD) is an autosomal-dominant, heritable skeletal and dental disease, involving hypoplastic clavicles, defective ossification of the anterior fontanelle, dentin and enamel hypoplasia, and supernumerary teeth, which can seriously affect the oral and… read more here.

Keywords: cleidocranial dysplasia; tooth hypoplasia; ccd; remineralization ... See more keywords

A Novel 90-kbp Deletion of RUNX2 Associated with Cleidocranial Dysplasia

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2 Published in 2022 at "Genes"

DOI: 10.3390/genes13071128

Abstract: 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, small or large fragment deletions are the common mutation types of… read more here.

Keywords: cleidocranial dysplasia; deletion runx2; dysplasia; kbp deletion ... See more keywords