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1.
J Learn Disabil ; 34(3): 286-93, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-15499882

RESUMO

The purpose of this study was to assess the predictive value of kindergarten teachers' ratings of pupils for later first-grade academic achievement. Kindergarten students were rated by their teachers on a variety of variables, including math and reading performance, teacher concerns, and amount of learning relative to peers. These variables were then analyzed with respect to outcome measures for math and reading ability administered in the first grade. The teachers' ratings of academic performance were significantly correlated with scores on the outcome measures. Analyses were also carried out to determine sensitivity, specificity, and predictive values of the different teacher ratings. The results indicated high overall accuracy, sensitivity, specificity, and negative predictive value for the ratings. Positive predictive value tended to be lower. A recommendation to follow from these results is that teacher ratings of this sort be used to determine which children should receive cognitive screening measures to further enhance identification of children at risk for learning disability. However, this recommendation is limited by the lack of empirically supported screening measures for math disability versus well-supported screening tools for reading disability.


Assuntos
Deficiências da Aprendizagem/diagnóstico , Baixo Rendimento Escolar , Criança , Transtornos do Comportamento Infantil/diagnóstico , Transtornos do Comportamento Infantil/psicologia , Pré-Escolar , Dislexia/diagnóstico , Dislexia/psicologia , Feminino , Humanos , Deficiências da Aprendizagem/psicologia , Estudos Longitudinais , Masculino , Matemática , Determinação da Personalidade/estatística & dados numéricos , Psicometria/estatística & dados numéricos , Leitura , Reprodutibilidade dos Testes , Medição de Risco
2.
Am J Med Genet ; 83(4): 281-5, 1999 Apr 02.
Artigo em Inglês | MEDLINE | ID: mdl-10208162

RESUMO

Parents of 55 preschool and school-aged children with the FMR1 full mutation (fM) completed a brief screening questionnaire. Parents of 55 additional children, each of whom was individually matched for sex, age, and IQ to one of the 55 children with Fragile X syndrome, also completed a questionnaire. Items on the questionnaire concerned behavior, rather than physical features or family history, associated with Fragile X syndrome. Children with the fM were more likely than controls to be on prescription medication, to have poor eye contact, to be described as nervous or anxious, and to regularly engage in repetitive movements and/or repetitive speech. Moreover, children with the fM received higher total scores on the questionnaire than their matched controls. These results suggest that questions about behavior are useful in the diagnostic evaluation of Fragile X syndrome, especially in the absence of the recognizable physical features associated with this condition.


Assuntos
Síndrome do Cromossomo X Frágil/diagnóstico , Inquéritos e Questionários/estatística & dados numéricos , Adolescente , Criança , Pré-Escolar , Feminino , Síndrome do Cromossomo X Frágil/psicologia , Humanos , Lactente , Testes de Inteligência , Masculino , Programas de Rastreamento/métodos , Fatores de Risco , Sensibilidade e Especificidade
3.
J Dev Behav Pediatr ; 18(6): 392-8, 1997 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9431501

RESUMO

The prevalence of the fragile X mental retardation (FMR) 1 and FMR2 full mutations (fM) was examined among 1014 school-age children with academic difficulties but without mental retardation. Both Southern blot and polymerase chain reaction analyses for FMR1 and FMR2 were performed on samples obtained from these children. No fM genes were found, and one FMR1 premutation was identified. The distribution of allele sizes for both genes was comparable to those reported for other clinical and normal population samples. These results suggest that neither the FMR1 nor the FMR2 mutation is a common etiology of academic failure among school-age children without mental retardation and that the prevalence of the FMR1 premutation is no more frequent in children with academic failure than it is in the general population.


Assuntos
Transtornos Cognitivos/diagnóstico , Transtornos Cognitivos/genética , Síndrome do Cromossomo X Frágil/genética , Mutação Puntual/genética , Baixo Rendimento Escolar , Cromossomo X , Alelos , Criança , Aberrações Cromossômicas , Transtornos Cromossômicos , Feminino , Síndrome do Cromossomo X Frágil/diagnóstico , Humanos , Testes de Inteligência , Masculino
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