Mafee M F, Schild J A, Kumar A, Valvassori G E, Pruzansky S
Int J Pediatr Otorhinolaryngol. 1984 Jul;7(3):229-38. doi: 10.1016/s0165-5876(84)80003-8.
Among the conditions that arise from disturbances in development of the first two branchial arches, the symmetric syndrome of mandibulofacial dysostosis and the asymmetric anomalies of the hemicraniofacial microsomia represent a characteristic pattern of craniofacial malformation distinct from other first and second arch syndromes. Since the usual embryonic aberration in both of these anomalies involves the first and second branchial arch derivatives, malformations of the external and middle ear are common. The external auditory canal is absent in the vast majority of the cases. Incudomallear deformities are usually present. In this paper, radiographic analysis of the ear-related developmental anomalies of 17 patients with mandibulofacial dysostosis is described.
在前两个鳃弓发育紊乱所引发的病症中,下颌面骨发育不全的对称综合征和半侧颅面短小畸形的不对称异常代表了一种独特的颅面畸形模式,有别于其他第一和第二鳃弓综合征。由于这两种异常情况中常见的胚胎畸变涉及第一和第二鳃弓衍生物,所以外耳和中耳畸形很常见。绝大多数病例中外耳道缺失。砧镫骨畸形通常存在。本文描述了17例下颌面骨发育不全患者耳部相关发育异常的影像学分析。