| Literature DB >> 16238657 |
Abstract
The authors describe the case of a 10-year-old girl presenting with Axenfeld-Rieger syndrome (ARS), a rare autosomal dominant condition. The patient showed severe hypodontia, microdontia and short roots. Early diagnosis of the syndrome from its dento-facial and systemic features is important so that subsequent ocular complications may be prevented.Entities:
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Year: 2005 PMID: 16238657 DOI: 10.1111/j.1365-263X.2005.00639.x
Source DB: PubMed Journal: Int J Paediatr Dent ISSN: 0960-7439 Impact factor: 3.455