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Article

Cleidocranial dysplasia: a family report.

Journal of the Indian Society of Pedodontics and Preventive Dentistry - 1 Jan 2000

Chelvan H Thamizh, Malathi N, Kailasam Vignesh, Ponnudurai A

Abstract excerpt

A 10-year-old girl presented with a chief complaint of many unerupted teeth. Complete clinical and radiological examination of this patient confirmed the diagnosis of cleidocranial dysplasia (CCD). Her father also presented similar features with a lesser clinical severity. CCD is an autosomal-dominant heritable skeletal disease caused by heterozygous mutations in the osteoblast-specific transcription factor RUNX2...

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Source

Identifiers

PMID: 19915277
DOI: 10.4103/0970-4388.57661

Genes

RUNX2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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