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1.
J Pediatr ; 154(4): 535-540.e1, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19185317

RESUMEN

OBJECTIVE: To test the hypothesis that children born preterm are more likely to screen positive on the M-CHAT for an autism spectrum disorder. STUDY DESIGN: We compared the M-CHAT positive rate of those with cerebral palsy, cognitive impairment, and vision and hearing impairments to those without such deficits. RESULTS: Relative to children who could walk, the odds for screening positive on the M-CHAT were increased 23-fold for those unable to sit or stand independently and more than 7-fold for those requiring assistance to walk. Compared with children without a diagnosis of cerebral palsy, those with quadriparesis were 13 times more likely to screen positive, and those with hemiparesis were 4 times more likely to screen positive. Children with major vision or hearing impairments were 8 times more likely to screen positive than those without such impairments. Relative to those with a Mental Development Index (MDI) of >70, the odds for screening positive were increased 13-fold for those with an MDI of <55 and more than 4-fold for those with an MDI of 55 to 69. CONCLUSIONS: Major motor, cognitive, visual, and hearing impairments appear to account for more than half of the positive M-CHAT screens in extremely low gestational age newborns. Even after those with such impairments were eliminated, 10% of children--nearly double the expected rate--screened positive.


Asunto(s)
Trastorno Autístico/prevención & control , Recien Nacido Prematuro , Recién Nacido de muy Bajo Peso , Tamizaje Masivo/métodos , Encuestas y Cuestionarios , Ceguera/psicología , Parálisis Cerebral/psicología , Preescolar , Trastornos del Conocimiento/psicología , Sordera/psicología , Reacciones Falso Positivas , Femenino , Humanos , Lactante , Recién Nacido , Modelos Logísticos , Masculino , Análisis Multivariante , Factores de Riesgo , Sensibilidad y Especificidad , Estados Unidos
2.
J Autism Dev Disord ; 38(8): 1426-38, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18188685

RESUMEN

One of the primary diagnostic criteria for the diagnosis of autism spectrum disorders (ASD) is the presence of a language delay or impairment. Children with ASD are now being identified at significantly younger ages, and prior research has consistently found that early language skills in this population are heterogeneous and an important predictor for later outcome. The goal of this study was to systematically investigate language in toddlers with ASD and to identify early correlates of receptive and expressive language in this population. The study included 164 toddlers with ASD between the ages of 18 and 33 months who were evaluated on several cognitive, language and behavioral measures. Results suggested good agreement among different measures of early language, including direct assessment and parent report measures. Significant concurrent predictors of receptive language included gestures, non-verbal cognitive ability and response to joint attention. For expressive language, the most significant predictors were non-verbal cognitive ability, gestures and imitation. These findings have important implications for intervention programs targeting this population.


Asunto(s)
Trastorno Autístico/diagnóstico , Trastornos del Desarrollo del Lenguaje/diagnóstico , Atención , Trastorno Autístico/psicología , Trastornos de la Conducta Infantil/diagnóstico , Trastornos de la Conducta Infantil/psicología , Preescolar , Trastornos del Conocimiento/diagnóstico , Trastornos del Conocimiento/psicología , Diagnóstico Precoz , Femenino , Gestos , Humanos , Conducta Imitativa , Lactante , Entrevista Psicológica , Trastornos del Desarrollo del Lenguaje/psicología , Pruebas del Lenguaje , Masculino , Tamizaje Masivo , Destreza Motora , Pruebas Neuropsicológicas , Juego e Implementos de Juego , Inteligibilidad del Habla , Percepción del Habla
3.
J Autism Dev Disord ; 37(1): 86-97, 2007 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17216333

RESUMEN

Although autism spectrum disorders (ASD) prevalence is higher in males than females, few studies address sex differences in developmental functioning or clinical manifestations. Participants in this study of sex differences in developmental profiles and clinical symptoms were 22 girls and 68 boys with ASD (mean age = 28 months). All children achieved strongest performance in visual reception and fine motor followed by gross motor and language functioning. Sex differences emerged in developmental profiles. Controlling for language, girls achieved higher visual reception scores than boys; boys attained higher language and motor scores and higher social-competence ratings than girls, particularly when controlling for visual reception. Longitudinal, representative studies are needed to elucidate the developmental and etiological significance of the observed sex differences.


Asunto(s)
Trastorno Autístico/epidemiología , Afecto , Trastorno Autístico/diagnóstico , Preescolar , Trastornos del Conocimiento/diagnóstico , Trastornos del Conocimiento/epidemiología , Discapacidades del Desarrollo/diagnóstico , Discapacidades del Desarrollo/epidemiología , Empatía , Femenino , Humanos , Lactante , Trastornos del Lenguaje/diagnóstico , Trastornos del Lenguaje/epidemiología , Masculino , Tamizaje Masivo/métodos , Trastornos de la Destreza Motora/diagnóstico , Trastornos de la Destreza Motora/epidemiología , Prevalencia , Distribución por Sexo , Conducta Social , Encuestas y Cuestionarios
4.
J Autism Dev Disord ; 36(3): 317-24, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16598435

RESUMEN

A multicenter study of 308 children with Autism Spectrum Disorder (ASD) was conducted through the Collaborative Programs of Excellence in Autism (CPEA), sponsored by the National Institute of Child Health and Human Development, to compare the family history of autoimmune disorders in children with ASD with and without a history of regression. A history of regression was determined from the results of the Autism Diagnostic Interview-Revised (ADI-R). Family history of autoimmune disorders was obtained by telephone interview. Regression was significantly associated with a family history of autoimmune disorders (adjusted OR=1.89; 95% CI: 1.17, 3.10). The only specific autoimmune disorder found to be associated with regression was autoimmune thyroid disease (adjusted OR=2.09; 95% CI: 1.28, 3.41).


Asunto(s)
Trastorno Autístico/epidemiología , Trastorno Autístico/genética , Regresión Psicológica , Tiroiditis Autoinmune , Niño , Demografía , Femenino , Humanos , Masculino , Factores de Riesgo , Tiroiditis Autoinmune/epidemiología , Tiroiditis Autoinmune/genética , Tiroiditis Autoinmune/psicología
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