| Syndrome of hajdu-cheney: three case reports of orofacial interest. | |
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MedLine Citation:
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PMID: 20500061 Owner: NLM Status: In-Data-Review |
Abstract/OtherAbstract:
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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. |
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Authors:
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E Vingerhoedt; I Bailleul-Forestier; P Fellus; J Schoenaers; J-P Frijns; C Carels |
Publication Detail:
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Type: Journal Article Date: 2010-03-01 |
Journal Detail:
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Title: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association Volume: 47 ISSN: 1545-1569 ISO Abbreviation: Cleft Palate Craniofac. J. Publication Date: 2010 Nov |
Date Detail:
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Created Date: 2010-11-02 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9102566 Medline TA: Cleft Palate Craniofac J Country: United States |
Other Details:
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Languages: eng Pagination: 645-53 Citation Subset: D; IM |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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