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1.
J Autism Dev Disord ; 52(5): 2149-2155, 2022 May.
Artículo en Inglés | MEDLINE | ID: mdl-34081298

RESUMEN

In March 2020, many schools were closed to prevent the spread of COVID-19 in Japan, and it is predicted that many children, especially those with neurodevelopmental disorders (NDDs), will be affected emotionally and behaviorally. Here, we examined the impact of school closures due to COVID-19 on school-aged children with NDDs using the Child Behavior Checklist. Totally, data on 121 children diagnosed with autism spectrum disorder, attention-deficit hyperactivity disorder, and/or intellectual disorder were analyzed and it was found that externalizing and aggressive behavior increased in all NDDs, regardless of the type of diagnosis. A clear prospect is important for children with NDDs children to lead a stable life, and more generous supports for children with NDDs and their families are needed.


Asunto(s)
Trastorno por Déficit de Atención con Hiperactividad , Trastorno del Espectro Autista , COVID-19 , Trastornos del Neurodesarrollo , Trastorno por Déficit de Atención con Hiperactividad/psicología , Trastorno del Espectro Autista/epidemiología , Trastorno del Espectro Autista/psicología , COVID-19/prevención & control , Niño , Humanos , Japón/epidemiología , Trastornos del Neurodesarrollo/diagnóstico , Trastornos del Neurodesarrollo/epidemiología , Trastornos del Neurodesarrollo/psicología
2.
J Autism Dev Disord ; 51(12): 4655-4662, 2021 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-33590427

RESUMEN

Although genetic factors are involved in the etiology of autism spectrum disorder (ASD), the significance of genetic analysis in clinical settings is unclear. Forty-nine subjects diagnosed with non-syndromic ASD were analyzed by microarray comparative genomic hybridization (CGH) analysis, whole-exome sequencing (WES) analysis, and panel sequencing analysis for 52 common causative genes of ASD to detect inherited rare variants. Genetic analysis by microarray CGH and WES analyses showed conclusive results in about 10% of patients, however, many inherited variants detected by panel sequencing analysis were difficult to interpret and apply in clinical practice in the majority of patients. Further improvement of interpretation of many variants detected would be necessary for combined genetic tests to be used in clinical settings.


Asunto(s)
Trastorno del Espectro Autista , Trastorno del Espectro Autista/diagnóstico , Trastorno del Espectro Autista/genética , Hibridación Genómica Comparativa , Variaciones en el Número de Copia de ADN , Predisposición Genética a la Enfermedad , Pruebas Genéticas , Genómica , Humanos
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