自闭症谱系障碍
医学
心理信息
检查表
背景(考古学)
梅德林
数据提取
荟萃分析
自闭症
临床心理学
物理医学与康复
精神科
心理学
古生物学
法学
认知心理学
内科学
生物
政治学
作者
Yi Huey Lim,Melissa K. Licari,Alicia J Spittle,Rochelle Watkins,Jill G. Zwicker,Jenny Downs,Amy Finlay‐Jones
出处
期刊:Pediatrics
[American Academy of Pediatrics]
日期:2021-02-01
卷期号:147 (2)
被引量:21
标识
DOI:10.1542/peds.2020-011270
摘要
CONTEXT: Early motor impairments have been reported in children with neurodevelopmental disorders (NDD), but it is not clear if early detection of motor impairments can identify children at risk for NDD or how early such impairments might be detected. OBJECTIVE: To characterize early motor function in children later diagnosed with NDD relative to typically developing children or normative data. DATA SOURCES: The Cumulative Index to Nursing and Allied Health Literature, Embase, Medline, PsycINFO, and Scopus electronic databases were searched. STUDY SELECTION: Eligible studies were required to include an examination of motor function in children (0–24 months) with later diagnosis of NDD by using standardized assessment tools. DATA EXTRACTION: Data were extracted by 4 independent researchers. The quality of the studies was assessed by using the Standard Quality Assessment Criteria for Evaluating Primary Research Papers from a Variety of Fields checklist. RESULTS: Twenty-five studies were included in this review; in most of the studies, the authors examined children with later autism spectrum disorder (ASD). Early motor impairments were detected in children later diagnosed with ASD. The meta-analysis results indicated that differences in fine, gross, and generalized motor functions between the later ASD and typically developing groups increased with age. Motor function across different NDD groups was found to be mixed. LIMITATIONS: Results may not be applicable to children with different types of NDD not reported in this review. CONCLUSIONS: Early motor impairments are evident in children later diagnosed with ASD. More research is needed to ascertain the clinical utility of motor impairment detection as an early transdiagnostic marker of NDD risk.
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