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先天性卵圆窗缺失。

Congenital absence of the oval window.

作者信息

Lambert P R

机构信息

Department of Otolaryngology, Head and Neck Surgery, University of Virginia Health Sciences Center, Charlottesville 29908.

出版信息

Laryngoscope. 1990 Jan;100(1):37-40. doi: 10.1288/00005537-199001000-00009.

Abstract

From 1983 to 1987, seven patients with conductive hearing loss were found to have congenital absence of the oval window. Six of these patients underwent vestibulotomies and reconstruction with House wires or total ossicular reconstruction prostheses. Surgical findings included absent or rudimentary stapes in all cases, abnormal facial nerves in four cases, and abnormal long processes of the incus in four cases. All patients had normal external ear canals and tympanic membranes. Hearing initially improved 20 to 45 dB in four of the six patients reconstructed. Over time, however, much of this initial hearing gain was lost. A marked difference in hearing results was evident between this series of absent oval window cases and a recent series of major atresia cases.

摘要

1983年至1987年期间,发现7例传导性听力损失患者存在先天性卵圆窗缺失。其中6例患者接受了前庭切开术,并使用豪斯钢丝或全听骨链重建假体进行重建。手术发现包括所有病例中镫骨缺失或发育不全,4例面神经异常,4例砧骨长突异常。所有患者外耳道和鼓膜均正常。6例接受重建的患者中,有4例听力最初提高了20至45分贝。然而,随着时间的推移,最初获得的大部分听力又丧失了。这一系列卵圆窗缺失病例与最近一系列严重闭锁病例的听力结果存在明显差异。

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