O'Dwyer E M, Jones D C
Department of Oral and Maxillofacial Surgery, Arrowe Park Hospital, Upton, UK.
Int J Paediatr Dent. 2005 Nov;15(6):459-63. doi: 10.1111/j.1365-263X.2005.00639.x.
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.
作者描述了一名患有Axenfeld-Rieger综合征（ARS）的10岁女孩的病例，这是一种罕见的常染色体显性疾病。该患者表现出严重的牙齿发育不全、小牙症和短根。从其牙面和全身特征对该综合征进行早期诊断很重要，以便预防随后的眼部并发症。
