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脆性 X 智力低下 1 型基因(FMR1)突变的行为表型。

The behavioral phenotype of FMR1 mutations.

机构信息

Kennedy Krieger Institute’s Fragile X Clinic, Baltimore, MD 21205, USA.

出版信息

Am J Med Genet C Semin Med Genet. 2010 Nov 15;154C(4):469-76. doi: 10.1002/ajmg.c.30277.

Abstract

The purpose of this article is to provide an overview of the behavioral phenotype of FMR1 mutations, including fragile X syndrome (FXS) in order to better understand the clinical involvement of individuals affected by mutations in this gene. FXS is associated with a wide range of intellectual and behavioral problems, some relatively mild and others quite severe. FXS is the most common cause of inherited intellectual disability and one of the most prevalent genetic causes of autism spectrum disorder. Learning difficulties, attentional problems, anxiety, aggressive behavior, stereotypies, and mood disorders are also frequent in FXS. Recent studies of children and adults have identified associations between FMR1 premutation and many of the same disorders. We examine the neurobehavioral phenotypes of FXS and FMR1 premutation as they manifest across the lifespan of the individual.

摘要

本文旨在概述 FMR1 突变的行为表型,包括脆性 X 综合征(FXS),以便更好地了解受该基因突变影响的个体的临床情况。FXS 与广泛的智力和行为问题相关,其中一些相对较轻,而另一些则较为严重。FXS 是遗传性智力障碍的最常见原因,也是自闭症谱系障碍最常见的遗传原因之一。学习困难、注意力问题、焦虑、攻击性行为、刻板行为和情绪障碍在 FXS 中也很常见。最近对儿童和成人的研究发现,FMR1 前突变与许多相同的疾病之间存在关联。我们研究了 FXS 和 FMR1 前突变在个体整个生命周期中的神经行为表型。

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