| Literature DB >> 20500061 |
E Vingerhoedt1, I Bailleul-Forestier, P Fellus, J Schoenaers, J-P Frijns, C Carels.
Abstract
Hajdu-Cheney syndrome is a rare, probably autosomal dominant connective tissue disorder with a variable expressivity. It is characterized by an osteoporotic skeleton, acro-osteolysis, a proportionate short stature, and distinctive orofacial anomalies. The aim of this article is to focus on the orofacial manifestations in two sporadic cases and one familial case with Hajdu-Cheney syndrome. Several common dental and craniofacial features are described. In contrast to earlier proposed diagnostic features, these patients show persisting deciduous teeth, problematic tooth eruption, and tendency toward a Class III malocclusion.Entities:
Mesh:
Year: 2010 PMID: 20500061 DOI: 10.1597/09-030
Source DB: PubMed Journal: Cleft Palate Craniofac J ISSN: 1055-6656