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Article

Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia.

Orthodontics & craniofacial research - 1 Nov 2010

Suda N, Hattori M, Kosaki K, Banshodani A, Kozai K, Tanimoto K, Moriyama K

Abstract excerpt

INTRODUCTION: Cleidocranial dysplasia (CCD, MIM#119600), for which the responsible gene is RUNX2, is a genetic disorder characterized by hypoplasia or aplasia of the clavicles, patent fontanelles, and a short stature. Supernumerary teeth and delayed eruption and impaction of permanent teeth are frequently associated with CCD. Our previous study reported wide intrafamilial variation in supernumerary tooth...

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Adenine
Cleidocranial Dysplasia
Core Binding Factor Alpha 1 Subunit
Diseases in Twins
Glutamine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Twins, Monozygotic

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PMID: 21040462
DOI: 10.1111/j.1601-6343.2010.01495.x

Genes

RUNX2

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