高嗜酸性粒细胞综合征患者Balínt综合征的发生

Philipp Klocke, A. Whalen-Browne, E. Hepworth, M. Panju
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引用次数: 0

摘要

Balínt综合征是一种后天性疾病,表现为无法同时识别多个物体(同时失语症),尽管运动功能完整,但视觉引导下的肢体运动不准确(视共济失调),以及尽管眼球运动范围不受限制,但无法对视觉目标进行准确的自主扫视(眼运动失用症)。在这里,我们报告了第一例由血小板衍生生长因子受体a突变(PDGFRA)诱导的高嗜酸性粒细胞综合征(HES)引起的Balínt综合征患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Occurrence of Balínt Syndrome in a Patient with Hypereosinophilic Syndrome
Balínt Syndrome is an acquired disorder manifesting in the inability to recognize several objects at once (simultagnosia), inaccurate visually guided limb movements despite intact motor function (optic ataxia) and the inability to make accurate voluntary saccades to visual targets despite demonstrating unrestricted range of eye movements (ocular motor apraxia). Here we report the first case of a patient presenting with Balínt Syndrome caused by a platelet-derived growth factor receptor A mutation (PDGFRA)-induced Hypereosinophilic Syndrome (HES).
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