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[注意缺陷多动障碍(ADHD)——分子与遗传方面]

[Attention deficit hyperactivity disorder (ADHD)--molecular and genetic aspects].

作者信息

Migdalska Anna, Nawara Magdalena, Bal Jerzy, Mazurczak Tadeusz

机构信息

Instytut Genetyki i Biotechnologii, Uniwersytet Warszawski, Warszawa, Poland.

出版信息

Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):343-54.

Abstract

Attention deficit hyperactivity disorder (ADHD) is a common neurobehavioral disorder of childhood, affecting approximately 5-10% of children. ADHD is considered to be a multifactorial disorder because both genetic and environmental components may contribute to its progress. The etiology of attention deficit hyperactivity disorder (ADHD) is unknown, however family, twin and adoption studies have suggested that genetic factors are very important in its etiopathogenesis. The research of genetic basis of ADHD consists of linkage analysis, candidate gene approach and association studies. These analyses and also investigations on animal models of disease suggest that mutations in genes involved in dopaminergic, serotonergic and adrenergic systems are likely to be responsible for ADHD.

摘要

注意缺陷多动障碍(ADHD)是一种常见的儿童神经行为障碍,约5-10%的儿童受其影响。ADHD被认为是一种多因素疾病,因为遗传和环境因素都可能促使其发展。注意缺陷多动障碍(ADHD)的病因尚不清楚,然而家族、双生子和收养研究表明,遗传因素在其发病机制中非常重要。ADHD遗传基础的研究包括连锁分析、候选基因法和关联研究。这些分析以及对疾病动物模型的研究表明,多巴胺能、血清素能和肾上腺素能系统相关基因的突变可能是ADHD的病因。

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