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家族性多小脑回畸形的语言和阅读技能特征

Characterization of language and reading skills in familial polymicrogyria.

作者信息

Oliveira Ecila Paula Mesquita, Hage Simone Rocha Vasconcelos, Guimarães Catarina Abraão, Brandão-Almeida Iara, Lopes-Cendes Iscia, Guerreiro Carlos Alberto, Teixeira Karine Couto Sarmento, Montenegro Maria Augusta, Cendes Fernando, Guerreiro Marilisa Mantovani

机构信息

Department of Neurology, FCM/Unicamp, Campinas, SP, Brazil.

出版信息

Brain Dev. 2008 Apr;30(4):254-60. doi: 10.1016/j.braindev.2007.08.010. Epub 2007 Oct 24.

Abstract

Polymicrogyria (PMG) is a malformation of cortical development characterized by an excessive number of small gyri and abnormal cortical lamination, giving the cortical surface an irregular and gross appearance. The severity of clinical manifestations correlates with the extent of cortical involvement. The objective of the present study was to describe three families with linguistic features of developmental language disorder and reading impairment, and to establish a neuroanatomic correlation through neuroimaging. Subjects have been submitted to a comprehensive protocol including psychological assessment, language evaluation, neurological examination, and neuroimaging investigation. In our families, children usually had the diagnosis of developmental language disorder while adults had the diagnosis of reading impairment. MRI showed perisylvian polymicrogyria in several subjects of each family. Our data support the idea that there is a co-occurrence of developmental language disorder and reading impairment and both conditions may be associated with polymicrogyria.

摘要

多小脑回畸形(PMG)是一种皮质发育畸形,其特征是存在过多的小脑回和异常的皮质分层,使皮质表面呈现不规则且粗糙的外观。临床表现的严重程度与皮质受累程度相关。本研究的目的是描述三个具有发育性语言障碍和阅读障碍语言特征的家系,并通过神经影像学建立神经解剖学关联。研究对象接受了包括心理评估、语言评估、神经学检查和神经影像学检查在内的综合方案。在我们研究的家系中,儿童通常被诊断为发育性语言障碍,而成年人则被诊断为阅读障碍。MRI显示每个家系的几名研究对象存在外侧裂周围多小脑回畸形。我们的数据支持这样一种观点,即发育性语言障碍和阅读障碍共同出现,且这两种情况都可能与多小脑回畸形有关。

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