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自闭症谱系障碍儿童的性别差异在高危婴儿队列中得到确认。

Sex differences in children with autism spectrum disorder identified within a high-risk infant cohort.

机构信息

Department of Pediatrics, University of Alberta, Edmonton, AB, Canada.

出版信息

J Autism Dev Disord. 2012 Dec;42(12):2585-96. doi: 10.1007/s10803-012-1515-y.

DOI:10.1007/s10803-012-1515-y
PMID:22453928
Abstract

Sex differences were examined in 3-year-olds with autism spectrum disorders (ASD) ascertained from a high-risk cohort, and high- and low-risk comparison groups. Participants included 319 high-risk siblings and 129 low-risk controls. Eighty-five siblings were diagnosed with ASD, including 57 of 176 boys (32.4 %) and 28 of 143 girls (19.6 %), implying a relative odds of ASD of 1.65 in boys versus girls. There were modest sex differences on cognitive and adaptive skills and ASD symptom severity at age 3, but differences between boys and girls with ASD mirrored those in the non-ASD groups. The lower than expected male-to-female ratio, and the relatively high cognitive level among diagnosed children, suggest that we have identified an unanticipated number of higher-functioning girls with ASD.

摘要

本研究对从高风险队列中确定的自闭症谱系障碍(ASD)的 3 岁儿童进行了性别差异研究,并设立了高风险和低风险对照组。研究参与者包括 319 名高风险兄弟姐妹和 129 名低风险对照组。85 名兄弟姐妹被诊断患有 ASD,其中 176 名男孩中有 57 名(32.4%),143 名女孩中有 28 名(19.6%),这表明男孩患 ASD 的相对风险是女孩的 1.65 倍。在 3 岁时,在认知和适应技能以及 ASD 症状严重程度方面存在性别差异,但 ASD 男孩和女孩之间的差异与非 ASD 组的差异相匹配。低于预期的男女性别比例,以及诊断出的儿童相对较高的认知水平,表明我们已经发现了数量意外的高功能女性 ASD 儿童。

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本文引用的文献

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Recognising and diagnosing autism in children and young people: summary of NICE guidance.识别和诊断儿童及青少年自闭症:英国国家卫生与临床优化研究所指南摘要
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Sex differences in autism spectrum disorder: evidence from a large sample of children and adolescents.自闭症谱系障碍中的性别差异:来自大量儿童和青少年样本的证据。
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Understanding strengths and challenges of people with autism: insights from parents and practitioners.了解自闭症患者的优势与挑战:来自家长和从业者的见解。
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7
Exploring the Acquisition of Social Communication Skills in Children with Autism: Preliminary Findings from Applied Behavior Analysis (ABA), Parent Training, and Video Modeling.探索自闭症儿童社交沟通技能的习得:应用行为分析(ABA)、家长培训和视频示范的初步结果。
Brain Sci. 2024 Feb 9;14(2):172. doi: 10.3390/brainsci14020172.
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May Female Autism Spectrum Be Masked by Eating Disorders, Borderline Personality Disorder, or Complex PTSD Symptoms? A Case Series.女性自闭症谱系障碍会被饮食失调、边缘型人格障碍或复杂性创伤后应激障碍症状掩盖吗?病例系列研究
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Global burden and inequality of autism spectrum disorders: Based on data from the 2019 Global Burden of Disease study.孤独症谱系障碍的全球负担与不平等:基于2019年全球疾病负担研究的数据。
Prev Med Rep. 2023 Nov 11;36:102511. doi: 10.1016/j.pmedr.2023.102511. eCollection 2023 Dec.
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为 12 至 47 个月大的幼儿和学龄前儿童自闭症谱系障碍的诊断,综合多个来源的信息。
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Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.使用 array CGH 检测自闭症家系基因组中的外显子拷贝数变异,发现 TMLHE 中的一个新缺失。
Hum Mol Genet. 2011 Nov 15;20(22):4360-70. doi: 10.1093/hmg/ddr363. Epub 2011 Aug 24.
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Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.Xp22.11 缺失:PTCHD1 是伴或不伴孤独症的 X 连锁智力障碍的候选基因。
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Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.Xp22.11 上的 PTCHD1 基因座缺失与自闭症谱系障碍和智力障碍。
Sci Transl Med. 2010 Sep 15;2(49):49ra68. doi: 10.1126/scitranslmed.3001267.
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De novo rates and selection of large copy number variation.从头开始的大拷贝数变异的发生率和选择。
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