Department of Pediatrics, University of Chieti, Chieti, Italy.
Epilepsy Behav. 2013 Jul;28(1):108-12. doi: 10.1016/j.yebeh.2013.04.005. Epub 2013 May 22.
To assess and characterize a possible neurocognitive endophenotype associated with Rolandic epilepsy (RE), a clinical study was carried out to evaluate the neuropsychological profile of children with RE at onset and of their healthy siblings. Seventeen subjects were recruited (10 boys and 7 girls): nine patients affected by RE and eight siblings who underwent clinical and neuropsychological evaluations. All patients and only two siblings showed centrotemporal spikes on the electroencephalographic recording. Eighteen age- and sex-matched healthy children were assessed as controls. A significant impairment was found in language domain, attentional functioning, and short- and long-term verbal memory in both patients and siblings. A positive correlation between verbal comprehension and working memory scores was found in both groups. A similar neuropsychological profile of RE, which affected patients and their siblings with impairment in the same developing areas, supports the hypothesis of a specific neurocognitive phenotype in RE.
为了评估与 Rolandic 癫痫(RE)相关的潜在神经认知表型并对其进行特征描述,开展了一项临床研究,以评估初发 RE 患儿及其健康兄弟姐妹的神经心理学特征。共招募了 17 名受试者(男 10 名,女 7 名):9 名患者患有 RE,8 名兄弟姐妹接受了临床和神经心理学评估。所有患者和仅两名兄弟姐妹的脑电图记录显示中央颞区棘波。18 名年龄和性别匹配的健康儿童作为对照组进行评估。患者和兄弟姐妹在语言领域、注意力功能以及短期和长期言语记忆方面均存在显著障碍。两组患者的言语理解和工作记忆评分呈正相关。RE 具有相似的神经心理学特征,患者及其兄弟姐妹在相同的发育领域受到影响,支持了 RE 存在特定神经认知表型的假说。