寻找Tic之间的共同点;强迫症和自闭症谱系障碍:第一部分,Tic障碍

J. Barnhill, J. Bedford, J. Crowley, T. Soda
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引用次数: 2

摘要

摘要本文是四篇旨在探讨自闭症谱系障碍(ASD)与自闭症谱系障碍(ASD)之间复杂相互关系的文章中的第一篇;强迫症及相关障碍(OCRD)和抽动障碍/图雷特综合症(TD/TS)。我们首先概述TD/TS,然后检讨OCRD和ASD。本系列的最后一篇文章综合了所有三种综合征患者共有的神经生物学和遗传标记。目的是描述这些患者的复杂内表型,以更好地定义这些异质性临床综合征的基因标记。抽动障碍(TD)是儿童早期开始的多动运动的集合。抽搐对大多数受影响的学龄前儿童来说是短暂的,但一个亚组发展为持续的运动或进展,发展为图雷特综合征(TS)。TDs作为一个群体具有很高的遗传率,但明确的基因标记仍然是未知的。定义遗传标记的困难在很大程度上是由于不同的神经发育轨迹,不断变化的地形和类型,广泛的神经认知和行为并发症的发展,以及精神合并症的混合模式。
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A search for the common ground between Tic; Obsessive-compulsive and Autism Spectrum Disorders: part I, Tic disorders
Abstract This article is the first of four articles designed to explore the complex interrelationship between Autism Spectrum Disorders (ASD); Obsessive compulsive and Related Disorders (OCRD) and Tic Disorders/Tourette's Syndrome (TD/TS). We begin with an overview TD/TS and follow-up with reviews of OCRD and ASD. The final article in this series represents a synthesis of the neurobiological and genetic markers shared by patients presenting with all three syndromes. The goal is to describe the complex endophenotype of these patients in an effort to better define gene markers that underlie these heterogeneous clinical syndromes. Tic disorders (TD) are a collection of hyperkinetic movements that begin in early childhood. Tics are transient for most affected preschool children but a subgroup development persistent movements or progress to develop Tourette Syndrome (TS). TDs as a group display high heritability rates but definitive gene markers still elude us. The difficulty defining genetic markers is in large part due to the diverse neurodevelopmental trajectory, changing topography and typology, development of a broad spectrum of neurocognitive and behavioral complications, and a mixed pattern of psychiatric comorbidities.
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AIMS Genetics
AIMS Genetics GENETICS & HEREDITY-
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