Kumar A, Chaudhary D, Gupta S K
Department of Pediatrics, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.
Australas Radiol. 1996 May;40(2):160-1. doi: 10.1111/j.1440-1673.1996.tb00373.x.
We report a case of the Wildervanck (cervico-oculo-acoustic) syndrome exhibiting Klippel-Feil anomaly, congenital sensorineural deafness and bilateral sixth nerve palsy. Associated anomalies included short stature, microcephaly, mental retardation, and cleft palate.
我们报告一例患有Wildervanck(颈-眼-耳)综合征的病例,该患者表现为Klippel-Feil畸形、先天性感音神经性耳聋和双侧第六脑神经麻痹。相关异常包括身材矮小、小头畸形、智力迟钝和腭裂。