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首页> 外文期刊>Brain & Development >Reading disability due to an ocular motor disorder: A case of an adolescent girl with a previous diagnosis of dyslexia
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Reading disability due to an ocular motor disorder: A case of an adolescent girl with a previous diagnosis of dyslexia

机译:由于眼电机障碍导致的阅读障碍:一种青春期女孩的案例,具有诊断综合症的诊断

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Dyslexia is a reading disability characterized by difficulties with accurate and/or fluent word recognition, which are thought to stem from a phonological processing impairment. Herein we report the case of a 13-year-old girl who received the diagnosis of dyslexia at age 12 years. We considered this diagnosis to be incorrect because her reading difficulty was caused by a spontaneously repeated eye movement toward the vertical direction; the eyes were likely to show slow, upward drifts followed by quick downward movement at the physical examination, and the amplitude of the downward movement was increased when she changed eye positions to look at the upper direction in the evaluation of the eye tracker. Although we considered there was the possibility that the spontaneously repeated eye movement was classified as the spontaneous downbeat nystagmus, the eye tracker showed the transition of the gaze starting from and returning to was inconsistent with nystagmus, and we concluded that the term of nystagmus like abnormal eye movement was appropriate for the expression of the spontaneously repeated eye movement. There was no apparent abnormality on head magnetic resonance imaging (MRI), and whole exome sequencing showed no known candidate genes to explain the cerebellar dysfunction. An accumulation of similar cases in the future should help elucidate the pathomechanism observed in this case, and we should fully pay attention to evaluate the neurological aspects of the patients before settling on the diagnosis of dyslexia. (C) 2018 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.
机译:阅读障碍是一种阅读障碍,其特点是具有准确和/或流畅的词识别的困难,这被认为是源于语音处理障碍。在此,我们举报了一个13岁女孩的案件,接受了12岁的诊断障碍。我们认为这种诊断是不正确的,因为她的阅读难度是由朝向垂直方向的自发反复的眼睛运动引起的;眼睛很可能显示缓慢,向上漂移,然后在物理检查时快速向下移动,并且当她改变眼睛位置以查看眼睛跟踪器的评估中的上方时,向下运动的幅度增加。虽然我们认为有可能被自发反复的眼球运动被归类为自发性下滑的眼球震颤,但眼跟踪器显示凝视从凝视从并返回的过渡与眼球震颤不一致,我们得出结论,术语,术语的基因分子眼睛运动适合于表达自发反复的眼球运动。在头部磁共振成像(MRI)上没有明显的异常,并且整个外壳测序显示未知候选基因以解释小脑功能障碍。在未来的积累应该有助于阐明在这种情况下观察到的土地机制,并且我们应该完全注意评估患者的神经系统方面在沉降诊断患有综合症症之前。 (c)2018年日本儿童神经病学会。 elsevier b.v出版。保留所有权利。

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