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先天性视交叉缺失:利用单眼闪光视觉诱发电位证明未交叉的视觉通路

Congenital absence of optic chiasm: demonstration of an uncrossed visual pathway using monocular flash visual evoked potentials.

作者信息

Brown Malcolm C, Southern Caroline L, Anbarasu Arangasamy, Kaye Stephen B, Fisher Anthony C, Hagan Richard P, Newman William D

机构信息

Department of Clinical Engineering, Royal Liverpool University Hospital, Liverpool, L7 8XP, UK.

出版信息

Doc Ophthalmol. 2006 Jul;113(1):1-4. doi: 10.1007/s10633-006-9005-1. Epub 2006 Aug 12.

Abstract

A 35 month old child was referred for electrophysiology testing with pendular nystagmus, corresponding head oscillations and reduced vision. Flash visual evoked potential (VEP) revealed large responses at the right occiput (but not the left occiput) from the right eye and similar large responses at only the left occiput from the left eye, indicating absent/deficient crossover at the chiasm. A magnetic resonance imaging (MRI) scan subsequently confirmed absence of the optic chiasm. There was no other evidence of midline brain defects. Her subsequent development to age 11 has been followed. The nystagmus has remained mainly horizontal but a torsional component was noted from age 5 years and described as see-saw at age 6 years. A small right esotropia was noted at 6 years and spectacles prescribed for low hypermetropic refractive error. Bilateral superior rectus recessions at age 7 years produced an improved head posture. Her visual acuity has remained stable at around 6/24 from age 4 years. No binocularity nor stereopsis has been demonstrated over subsequent visits.

摘要

一名35个月大的儿童因摆动性眼球震颤、相应的头部摆动和视力下降被转诊进行电生理检查。闪光视觉诱发电位(VEP)显示右眼在右侧枕叶(而非左侧枕叶)有大的反应,左眼仅在左侧枕叶有类似的大反应,表明视交叉处交叉缺失/不足。随后的磁共振成像(MRI)扫描证实视交叉缺失。没有其他中线脑缺陷的证据。对她随后到11岁的发育情况进行了跟踪。眼球震颤主要仍为水平性,但5岁时出现了扭转成分,6岁时被描述为跷跷板样。6岁时发现有小的右眼内斜视,并因轻度远视性屈光不正而配戴眼镜。7岁时进行双侧上直肌后徙术,改善了头部姿势。自4岁起,她的视力一直稳定在约6/24。在随后的就诊中未发现双眼视或立体视。

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