Measurement considerations in pediatric research on autism spectrum disorders

被引:1
作者
Walsh, Karin S. [1 ,2 ]
Rau, Srishti [3 ]
机构
[1] Childrens Natl Hlth Syst, Washington, DC 20010 USA
[2] George Washington Univ, Sch Med, Washington, DC 20052 USA
[3] Childrens Natl Hlth Syst, Neuropsychol, Washington, DC USA
来源
GENETIC MODELS AND MOLECULAR PATHWAYS UNDERLYING AUTISM SPECTRUM DISORDERS | 2018年 / 241卷
关键词
Autism spectrum disorder; Assessment; Diagnosis; Genetic syndromes; Neurofibromatosis; Clinical research; ELEMENTARY-SCHOOL-AGE; NEUROFIBROMATOSIS TYPE-1; YOUNG-CHILDREN; DIAGNOSTIC INTERVIEW; COMORBID PSYCHOPATHOLOGY; INTELLECTUAL DISABILITY; PSYCHIATRIC-DISORDERS; ASPERGER-SYNDROME; BIPOLAR DISORDER; PARENT INTERVIEW;
D O I
10.1016/bs.pbr.2018.09.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Studying Autism Spectrum Disorders (ASD) in genetic syndromes has gained interest in the scientific community as a way to elucidate mechanisms and symptom profiles to understand ASD more broadly. Appropriate and adequate measurement of constructs, symptomatology, and outcomes in clinical research is of vital importance in establishing the prevalence of such symptoms and measuring change in symptoms in the context of clinical trials. As such, we provide an overview of the prevalence of ASD, present current diagnostic guidelines, discuss important comorbidities to consider, describe current assessment strategies in assessing ASD, and discuss these within the context of a specific genetic condition to highlight how ASD can be best evaluated.
引用
收藏
页码:193 / 220
页数:28
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