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抽动秽语综合征、注意力缺陷障碍、学习障碍、言语障碍和口吃之间的家族关系。

Familial relationship between Gilles de la Tourette's syndrome, attention deficit disorder, learning disabilities, speech disorders, and stuttering.

作者信息

Pauls D L, Leckman J F, Cohen D J

机构信息

Child Study Center, Yale University School of Medicine, New Haven, CT 06510.

出版信息

J Am Acad Child Adolesc Psychiatry. 1993 Sep;32(5):1044-50. doi: 10.1097/00004583-199309000-00025.

Abstract

OBJECTIVE

This study examined the familial relationship between Gilles de la Tourette's syndrome (GTS) and attention deficit disorder (ADD), learning problems, speech disorders, and stuttering.

METHOD

This family study consisted of 338 first degree relatives of 85 GTS probands and 113 controls. All available relatives were personally assessed using structured interviews, and family history information was collected from all family members. Best-estimate diagnoses were assigned for GTS, ADD, learning problems, speech disorders, and stuttering. Analyses examined whether ADD, learning problems, speech disorders, and stuttering by themselves represent genetically variant expressions of GTS.

RESULTS

There was no evidence that ADD, learning problems, speech disorders, or stuttering represent variant expressions of GTS. However, relatives with GTS were at increased risk for ADD regardless of the ADD diagnosis of the GTS proband.

CONCLUSIONS

ADD, learning problems, stuttering, and speech problems by themselves are not variant forms of GTS. However, GTS and ADD may be etiologically related in some persons. There may be two types of individuals with GTS and ADD: ones in whom ADD is independent of GTS, and others in whom ADD is secondary to occurrence of GTS.

摘要

目的

本研究探讨了抽动秽语综合征(GTS)与注意力缺陷障碍(ADD)、学习问题、言语障碍和口吃之间的家族关系。

方法

这项家族研究包括85名GTS先证者的338名一级亲属和113名对照。所有可及的亲属均通过结构化访谈进行个人评估,并从所有家庭成员处收集家族史信息。对GTS、ADD、学习问题、言语障碍和口吃进行最佳估计诊断。分析检查了ADD、学习问题、言语障碍和口吃本身是否代表GTS的基因变异表现。

结果

没有证据表明ADD、学习问题、言语障碍或口吃代表GTS的变异表现。然而,无论GTS先证者的ADD诊断如何,患有GTS的亲属患ADD的风险都会增加。

结论

ADD、学习问题、口吃和言语问题本身并非GTS的变异形式。然而,GTS和ADD在某些人身上可能存在病因学关联。可能存在两种患有GTS和ADD的个体:一种是ADD独立于GTS的个体,另一种是ADD继发于GTS发生的个体。

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