Van Doorne L, Wackens G, De Maeseneer M, Deron P
Department of Oral and Maxillofacial Surgery, Free University of Brussels, Belgium.
Int J Oral Maxillofac Surg. 1998 Apr;27(2):121-4. doi: 10.1016/s0901-5027(98)80309-3.
A 12-year-old boy with characteristic findings of otodental syndrome is presented. Abnormalities of deciduous and permanent dentition included bulbous canines, globe-shaped posterior teeth and agenesis of maxillary premolars. High-frequency sensorineural hearing loss was demonstrated, and results of genetic studies indicated an autosomal dominant trait. This patient presented previously unreported findings, including generalized macrodontia, delayed mineralization of the mandibular premolars, and supplementary permanent maxillary canines.
本文报告了一名患有耳牙综合征典型症状的12岁男孩。乳牙和恒牙的异常包括球根状犬齿、球形后牙以及上颌前磨牙缺失。已证实存在高频感音神经性听力损失，基因研究结果表明为常染色体显性性状。该患者出现了此前未报告的症状，包括全身性巨牙症、下颌前磨牙矿化延迟以及额外的上颌恒犬齿。
