Suppr超能文献

儿童注意缺陷多动障碍的生化和遗传学分析。

Biochemical and genetic analyses of childhood attention deficit/hyperactivity disorder.

机构信息

Department of Biochemistry, School of Health, Karatekin University, Cankiri, Turkey.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2012 Sep;159B(6):613-27. doi: 10.1002/ajmg.b.32077. Epub 2012 Jul 23.

Abstract

Attention deficit/hyperactivity disorder (ADHD) in children is a neurobehavioral disorder characterized by inattention, hyperactivity, and/or impulsivity. The biochemical abnormalities and genetic factors play significant roles in the etiology of ADHD. These symptoms affect the behavior performance and social relationships of children in school and at home. Recently, many studies about biochemical abnormalities in ADHD have been published. Several research groups have also suggested the genetic contribution to ADHD, and attempted to identify susceptibility and candidate genes for this disorder through the genetic linkage and association studies. To date, these studies have reported substantial evidence implicating several genes (dopaminergic: DRD4, DAT1, DRD5, COMT; noradrenergic: DBH, ADRA2A; serotonergic: 5-HTT, HTR1B, HTR2A; cholinergic: CHRNA4, and central nervous system development pathway: SNAP25, BDNF) in the etiology of ADHD. Understanding the biochemistry and genetics of ADHD will allow us to provide a useful addition with other treatment procedures for ADHD.

摘要

儿童注意缺陷多动障碍(ADHD)是一种神经行为障碍,其特征是注意力不集中、多动和/或冲动。生化异常和遗传因素在 ADHD 的发病机制中起着重要作用。这些症状会影响儿童在学校和家庭中的行为表现和人际关系。最近,许多关于 ADHD 生化异常的研究已经发表。一些研究小组还提出了 ADHD 的遗传贡献,并试图通过遗传连锁和关联研究来确定该疾病的易感基因和候选基因。迄今为止,这些研究报告了大量证据,表明了几个基因(多巴胺能:DRD4、DAT1、DRD5、COMT;去甲肾上腺素能:DBH、ADRA2A;5-羟色胺能:5-HTT、HTR1B、HTR2A;胆碱能:CHRNA4 和中枢神经系统发育途径:SNAP25、BDNF)在 ADHD 的发病机制中起作用。了解 ADHD 的生物化学和遗传学将使我们能够为 ADHD 提供其他治疗方法的有用补充。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验