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1.
Behav Genet ; 42(2): 287-98, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21870177

RESUMO

As individuals with chromosome 22q11.2 deletion syndrome (22q11DS) show a wide range of IQs, intellectual heterogeneity could mask the neuropsychological profile of the syndrome. This study was designed to identify specific neuropsychological features of children and adolescents with 22q11DS by taking into account the possible source of variability deriving from intellectual disability (ID). First, we compared several neuropsychological domains involving linguistic, visual-motor/visual-perceptual and memory abilities in 34 children and adolescents with 22q11DS and 83 mental age-matched typically developing (TD) participants. Then, we selected participants with 22q11DS according to whether or not they had ID and compared their neuropsychological profiles with those of chronological age-matched TD controls. Although language and several aspects of memory have been found impaired only in children with 22q11DS with ID, deficits in visual-spatial abilities and visual-object short-term memory persist in participants without ID and might be considered a characteristic of 22q11DS, not just related to the presence of ID. On the basis of our findings, children and adolescents with 22q11DS cannot be considered as a single group with a homogeneous neuropsychological profile and must be studied in relation to their global intellectual abilities.


Assuntos
Síndrome da Deleção 22q11/complicações , Síndrome da Deleção 22q11/psicologia , Deficiência Intelectual/genética , Adolescente , Criança , Pré-Escolar , Feminino , Humanos , Inteligência/genética , Itália , Masculino , Testes Neuropsicológicos , Fenótipo
2.
Neuropsychology ; 18(1): 29-37, 2004 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-14744185

RESUMO

This article describes the relationship between reading, phonological awareness abilities (PA), and intelligence in a group of 16 individuals with Williams syndrome (WS) and in a group of 16 typically developing children, matched for mental age. The individuals with WS were impaired in passage comprehension, in some areas of PA investigated (syllable deletion and rhyme detection), and in nonword reading accuracy, a measure of grapheme-phoneme conversion. This latter finding is relevant, considering that in Italy regular print-to-sound correspondence is the most practiced teaching routine in the early phases of learning to read.


Assuntos
Conscientização , Fonética , Leitura , Síndrome de Williams/fisiopatologia , Adolescente , Adulto , Transtornos da Articulação/etiologia , Transtornos da Articulação/fisiopatologia , Estudos de Casos e Controles , Criança , Compreensão/fisiologia , Feminino , Humanos , Testes de Linguagem , Masculino , Psicolinguística , Síndrome de Williams/complicações
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