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Article

[Cleidocranial dysplasia. Description and analysis of a patient cohort].

Mund-, Kiefer- und Gesichtschirurgie : MKG - 1 Nov 2006

Baumert U, Golan I, Driemel O, Reichert T E, Reicheneder C, Muessig D, Rose E

Abstract excerpt

BACKGROUND: Cleidocranial dysplasia (CCD) is a rare dysplasia of bony and dental tissue. Characteristic are typical craniofacial and dental findings including morphological anomalies. CCD is possibly the only general syndrome that can be diagnosed based on the dental findings alone. CCD correlates with mutations in the RUNX2 gene. PURPOSE: The present interdisciplinary study correlates phenotypic findings with...

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Source

Identifiers

PMID: 17051365
DOI: 10.1007/s10006-006-0029-1

Genes

RUNX2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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