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后天性内斜视作为阿诺德-奇阿利畸形的初始表现

Acquired esotropia as initial manifestation of Arnold-Chiari malformation.

作者信息

Bixenman W W, Laguna J F

出版信息

J Pediatr Ophthalmol Strabismus. 1987 Mar-Apr;24(2):83-6. doi: 10.3928/0191-3913-19870301-08.

Abstract

A 13-year-old patient originally presented with a divergence palsy and gaze-evoked nystagmus. Over a short period of time, the esotropia became increasingly comitant and was successfully treated with strabismus surgery. Three years later, she developed downbeat nystagmus. An Arnold-Chiari Malformation could only be demonstrated using nuclear magnetic resonance imaging (MRI). Subsequent neurosurgical decompression resulted in resolution of the downbeat nystagmus with maintenance of single binocularity.

摘要

一名13岁患者最初表现为散开性麻痹和凝视诱发性眼球震颤。在短时间内,内斜视变得越来越共同性,并通过斜视手术成功治疗。三年后,她出现了下跳性眼球震颤。仅通过核磁共振成像(MRI)才能显示出阿诺德-奇亚里畸形。随后的神经外科减压术使下跳性眼球震颤消失,并维持了双眼单视。

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