Suppr超能文献

自闭症的早期诊断及其对预后的影响:叙述性综述。

Early diagnosis of autism and impact on prognosis: a narrative review.

机构信息

Gillberg Neuropsychiatry Centre, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

出版信息

Clin Epidemiol. 2013;5:33-43. doi: 10.2147/CLEP.S41714. Epub 2013 Feb 21.

Abstract

Autism spectrum disorders involve a set of clinical phenotypes that mirror an early onset of neurodevelopmental deviations, with core symptoms that can probably be related to a deficiency in the social instinct. Underlying the cognitive impairments there are physiological brain problems, caused by a large number of medical factors. This narrative review of systematic reviews and meta-analyses from the last 5 years (2008-2012) presents aspects from many areas in autism spectrum disorder research, with a particular focus on early intervention and the subsequent impact on prognosis. Other major areas discussed are epidemiology, early symptoms and screening, early diagnosis, neuropsychology, medical factors, and the existence of comorbidities. There is limited evidence that any of the broadband "early intervention" programs are effective in changing the natural long-term outcome for many individuals with an early diagnosis of autism. However, there is some evidence that Early Intensive Behavioral Intervention (EIBI) is an effective treatment for some children with ASD. Nevertheless, there is emerging consensus that early diagnosis and information are needed in order that an autism-friendly environment be "created" around affected individuals.

摘要

自闭症谱系障碍涉及一组临床表型,反映了神经发育早期偏差,其核心症状可能与社交本能缺陷有关。在认知障碍的背后,有许多生理上的大脑问题,是由大量的医学因素引起的。本综述对过去 5 年(2008-2012 年)的系统评价和荟萃分析进行了叙述,介绍了自闭症谱系障碍研究的许多领域的方面,特别关注早期干预及其对预后的后续影响。讨论的其他主要领域包括流行病学、早期症状和筛查、早期诊断、神经心理学、医学因素以及合并症的存在。有有限的证据表明,任何宽带“早期干预”计划都能有效改变许多早期被诊断为自闭症的个体的自然长期预后。然而,有一些证据表明,早期密集行为干预(EIBI)是治疗自闭症儿童的有效方法。尽管如此,人们越来越一致认为,需要早期诊断和信息,以便在受影响的个体周围“创建”一个自闭症友好的环境。

相似文献

6
The future of Cochrane Neonatal.考克兰新生儿协作网的未来。
Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12.

引用本文的文献

本文引用的文献

8
10
The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome).22q13.3缺失综合征(费兰-麦克德米德综合征)
Mol Syndromol. 2012 Apr;2(3-5):186-201. doi: 10.1159/000334260. Epub 2011 Nov 22.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验