Brain & development · 2007
Characterization of language and reading skills in familial polymicrogyria.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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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
Аннотация
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.