儿童自闭症谱系障碍:主要问题及解决方法

N. V. Filippova, Y. Barylnik, M. A. Kamyshonkova, E. A. Atapina
{"title":"儿童自闭症谱系障碍:主要问题及解决方法","authors":"N. V. Filippova, Y. Barylnik, M. A. Kamyshonkova, E. A. Atapina","doi":"10.33920/med-01-2308-01","DOIUrl":null,"url":null,"abstract":"In recent decades, there has been an increase in the number of children suffering from autism spectrum disorders (ASD) all over the world, which determines the high relevance of early diagnosis of these disorders for timely treatment and correction. However, the diagnostic criteria for ASD require the assessment of certain psychomotor skills in a child, which mature much later than necessary for timely diagnosis, so quite often the final diagnosis is made only by 5–7 years. New clinical guidelines suggest that primary screening should be performed by a pediatrician, but practice shows that this does not happen in reality. The reasons for this are not only the contradictions in the diagnostic criteria, but also the current ICD-10 classification, which does not fully reflect the pathogenetic processes in the child's body. In the meantime, new clinical guidelines recognize the role of genetic disorders and epigenetic factors in the development of autism spectrum disorders. Currently, there are more than 100 genes associated with ASD. That is why autism spectrum disorders must be considered from the point of view of pathogenetic changes in the child's body, in many cases of a hereditary nature, which will allow offering timely and effective methods of diagnosis,treatment, and correction.","PeriodicalId":447580,"journal":{"name":"Vestnik nevrologii, psihiatrii i nejrohirurgii (Bulletin of Neurology, Psychiatry and Neurosurgery)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Autism spectrum disorders in children: main problems and solutions\",\"authors\":\"N. V. Filippova, Y. Barylnik, M. A. Kamyshonkova, E. A. Atapina\",\"doi\":\"10.33920/med-01-2308-01\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In recent decades, there has been an increase in the number of children suffering from autism spectrum disorders (ASD) all over the world, which determines the high relevance of early diagnosis of these disorders for timely treatment and correction. However, the diagnostic criteria for ASD require the assessment of certain psychomotor skills in a child, which mature much later than necessary for timely diagnosis, so quite often the final diagnosis is made only by 5–7 years. New clinical guidelines suggest that primary screening should be performed by a pediatrician, but practice shows that this does not happen in reality. The reasons for this are not only the contradictions in the diagnostic criteria, but also the current ICD-10 classification, which does not fully reflect the pathogenetic processes in the child's body. In the meantime, new clinical guidelines recognize the role of genetic disorders and epigenetic factors in the development of autism spectrum disorders. Currently, there are more than 100 genes associated with ASD. That is why autism spectrum disorders must be considered from the point of view of pathogenetic changes in the child's body, in many cases of a hereditary nature, which will allow offering timely and effective methods of diagnosis,treatment, and correction.\",\"PeriodicalId\":447580,\"journal\":{\"name\":\"Vestnik nevrologii, psihiatrii i nejrohirurgii (Bulletin of Neurology, Psychiatry and Neurosurgery)\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-08-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Vestnik nevrologii, psihiatrii i nejrohirurgii (Bulletin of Neurology, Psychiatry and Neurosurgery)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.33920/med-01-2308-01\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vestnik nevrologii, psihiatrii i nejrohirurgii (Bulletin of Neurology, Psychiatry and Neurosurgery)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33920/med-01-2308-01","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

近几十年来,世界范围内患有自闭症谱系障碍(ASD)的儿童数量不断增加,这决定了早期诊断这些疾病对及时治疗和纠正的高度相关性。然而,ASD的诊断标准要求对儿童的某些精神运动技能进行评估,这些技能的成熟远远晚于及时诊断所必需的时间,因此往往要到5-7岁才能做出最终诊断。新的临床指南建议初级筛查应由儿科医生进行,但实践表明,这在现实中并没有发生。造成这种情况的原因不仅是诊断标准的矛盾,而且目前的ICD-10分类并没有充分反映儿童体内的发病过程。与此同时,新的临床指南认识到遗传疾病和表观遗传因素在自闭症谱系障碍发展中的作用。目前,有超过100个基因与ASD相关。这就是为什么必须从儿童身体的致病变化的角度来考虑自闭症谱系障碍,在许多情况下是遗传性的,这将允许提供及时有效的诊断、治疗和纠正方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Autism spectrum disorders in children: main problems and solutions
In recent decades, there has been an increase in the number of children suffering from autism spectrum disorders (ASD) all over the world, which determines the high relevance of early diagnosis of these disorders for timely treatment and correction. However, the diagnostic criteria for ASD require the assessment of certain psychomotor skills in a child, which mature much later than necessary for timely diagnosis, so quite often the final diagnosis is made only by 5–7 years. New clinical guidelines suggest that primary screening should be performed by a pediatrician, but practice shows that this does not happen in reality. The reasons for this are not only the contradictions in the diagnostic criteria, but also the current ICD-10 classification, which does not fully reflect the pathogenetic processes in the child's body. In the meantime, new clinical guidelines recognize the role of genetic disorders and epigenetic factors in the development of autism spectrum disorders. Currently, there are more than 100 genes associated with ASD. That is why autism spectrum disorders must be considered from the point of view of pathogenetic changes in the child's body, in many cases of a hereditary nature, which will allow offering timely and effective methods of diagnosis,treatment, and correction.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Etiology and pathogenesis of mental disorders in patients with multiple sclerosis: anxiety, psychotic, and personality disorders, chemical addictions, pathological affect Neurosurgical approach to the treatment of otorhinogenic brain abscess (a clinical case) Role of neurotrophic growth factors in vincristine polyneuropathy in children with acute lymphoblastic leukemia Ultrasound assessment of blood flow in the median nerve in normal conditions and in carpal tunnel syndrome A correlation between anxiety-depressive symptoms and immune-metabolic parameters in patients with mixed anxiety and depressive disorder
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1