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罗兰多癫痫患儿及其亲属的听觉处理特定缺陷。

A specific deficit of auditory processing in children with Rolandic Epilepsy and their relatives.

作者信息

Smith Anna B, Dawes Piers, Smith Stuart, Pal Deb K

机构信息

King's College London, UK.

University of Manchester, UK.

出版信息

Epilepsy Behav. 2017 Jul;72:135-139. doi: 10.1016/j.yebeh.2017.04.043. Epub 2017 Jun 7.

Abstract

Previous research shows that children with Rolandic Epilepsy have deficits of auditory processing. We wanted to confirm the nature of this deficit and whether it aggregates in families. We compared 40 children with Rolandic Epilepsy and 32 unaffected siblings with 99 typically developing children and 71 parents of RE children with 31 healthy adults on a battery of auditory processing tests. We also examined ear advantage in children with RE, their siblings and parents using population norms and measured non-word reading performance. We found a specific deficit for competing words in patients, their siblings and their parents, suggesting that this particular impairment of auditory processing present in children with RE, is heritable and likely to be persistent. Importantly, scores on this subtest in patients and siblings were significantly correlated with non-word reading performance. We saw increased rates of atypical left ear advantage in patients and siblings but no evidence of this in parents. We present these findings as evidence of familial incidence of dichotic listening and ear advantage abnormalities in relatives of children with Rolandic Epilepsy.

摘要

先前的研究表明,患有罗兰多癫痫的儿童存在听觉处理缺陷。我们想要确认这种缺陷的本质以及它是否在家族中聚集。我们对40名患有罗兰多癫痫的儿童和32名未受影响的兄弟姐妹,与99名发育正常的儿童以及71名患有罗兰多癫痫儿童的父母和31名健康成年人进行了一系列听觉处理测试。我们还使用群体常模检查了患有罗兰多癫痫的儿童、他们的兄弟姐妹和父母的耳优势,并测量了非词阅读表现。我们发现患者、他们的兄弟姐妹和父母在竞争性词语方面存在特定缺陷,这表明患有罗兰多癫痫的儿童中存在的这种特定听觉处理损伤是可遗传的,并且可能会持续存在。重要的是,患者和兄弟姐妹在该子测试中的得分与非词阅读表现显著相关。我们发现患者和兄弟姐妹中存在非典型左耳优势的比例增加,但在父母中没有这种迹象。我们将这些发现作为患有罗兰多癫痫儿童的亲属中双耳分听和耳优势异常的家族发病率的证据。

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