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首页> 外文期刊>Epilepsy & behavior: E&B >Neuropsychological abnormalities in children with the Panayiotopoulos syndrome point to parietal lobe dysfunction
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Neuropsychological abnormalities in children with the Panayiotopoulos syndrome point to parietal lobe dysfunction

机译:Panayiotopoulos综合征患儿的神经心理学异常提示顶叶功能异常

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摘要

Panayiotopoulos syndrome (PS) is a common epilepsy syndrome associated with rare clinical seizures and unknown localization of the epileptogenic area. Despite findings of normal development in patients with PS, recent neuropsychological studies point to subtle and diverse cognitive impairments. No well-outlined hypothesis about the localization of the brain dysfunction responsible for these impairments has been proposed. We further explored the cognitive dysfunctions in PS and made inferences on the most likely anatomical localization of brain impairment. A group of 19 patients (aged 6-12) with PS was rated according to spike activity and lateralization. The patients were submitted to a neuropsychological evaluation to assess general intelligence, memory, language, visual-perceptual abilities, attention, and executive functions. Using 35-channel scalp EEG recordings, the N170 face-evoked event-related potential (ERP) was obtained to assess the functional integrity of the ventral pathway. All patients with PS showed normal IQ but subtle and consistent neurocognitive impairments. Namely, we found abnormalities in the copy task of the Rey-Osterrieth Complex Figure and in the Narrative Memory Test. There was no correlation between neuropsychological impairments with spike activity and hemispheric spike lateralization. The N170 ERP was normal in all patients except for one. Our neuropsychological findings demonstrate impairments in visual-perceptual abilities and in semantic processing. These findings, paired with the absence of occipital lobe dysfunction in all neuropsychological studies of PS performed to this date, support the existence of parietal lobe dysfunction.
机译:Panayiotopoulos综合征(PS)是一种常见的癫痫综合征,伴有罕见的临床癫痫发作和致癫痫区域的未知定位。尽管发现PS患者发展正常,但最近的神经心理学研究指出,认知障碍存在细微而多样的变化。尚未提出关于引起这些损害的脑功能障碍的局限性的概述。我们进一步探讨了PS的认知功能障碍,并推断出最可能的脑损伤的解剖学定位。根据峰值活动和偏侧性对一组19名6-12岁的PS患者进行了评分。患者接受了神经心理学评估,以评估其一般智力,记忆力,语言,视觉感知能力,注意力和执行功能。使用35通道头皮脑电图记录,获得了N170面部诱发的事件相关电位(ERP)以评估腹侧通路的功能完整性。所有PS患者均表现出正常的智商,但存在细微而持续的神经认知障碍。即,我们在Rey-Osterrieth Complex Figure的复制任务和叙事记忆测试中发现了异常。神经心理障碍与峰值活动和半球峰值偏侧化之间没有相关性。除一名患者外,所有患者的N170 ERP均正常。我们的神经心理学发现表明视觉感知能力和语义加工受到损害。这些发现与迄今为止进行的所有PS的神经心理学研究中都没有枕叶功能障碍相吻合,支持了顶叶功能障碍的存在。

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