THE IMPACT OF A SYNDROMAL DIAGNOSIS ON SURGERY FOR CONGENITAL MINOR EAR ANOMALIES

被引:22
作者
CREMERS, CWRJ
TEUNISSEN, E
机构
[1] Institute of Otorhinolaryngology, University Hospital of Nijmegen, Nijmegen
关键词
CONGENITAL DEAFNESS; STAPES ANKYLOSIS; BRANCHIOOTORENAL SYNDROME; KLIPPEL-FEIL SYNDROME; STAPES GUSHER SYNDROME; TREACHER-COLLINS SYNDROME; CRANIOSYNOSTOSIS; PFEIFFER SYNDROME; CROUZON SYNDROME;
D O I
10.1016/0165-5876(91)90097-U
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Between 1964 and 1986, 107 ears of 86 patients with a minor congenital ear anomaly underwent an exploratory tympanotomy at the Institute of Otorhinolaryngology of the University Hospital Nijmegen. A classification of these anomalies is proposed based on the surgical findings and results. The 4 groups in this classification are: isolated stapes ankylosis, stapes ankylosis associated with an anomaly of the malleus and incus, an isolated anomaly of the malleus and incus with a mobile stapes footplate and finally, aplasia of the oval and/or round window. In a total of 29 ears (22 patients) out of these 104 ears, the anomaly formed part of a syndrome. The various syndromes and the anomalies encountered are discussed. The impact of a syndromal diagnosis on the outcome of reconstructive ear surgery is discussed per syndrome.
引用
收藏
页码:59 / 74
页数:16
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