Characterizing associations and dissociations between anxiety, social, and cognitive phenotypes of Williams syndrome

被引:13
作者
Ng, Rowena [1 ,2 ]
Jaervinen, Anna [1 ]
Bellugi, Ursula [1 ]
机构
[1] Salk Inst Biol Studies, Cognit Neurosci Lab, La Jolla, CA 92037 USA
[2] Univ Minnesota, Inst Child Dev, Minneapolis, MN 55455 USA
关键词
Anxiety; Williams syndrome; Neurodevelopmental disorder; Maladaptive behaviors; Intellectual impairment; Social behavior; LONGITUDINAL COURSE; GENETIC INFLUENCES; CHILDREN; BEHAVIOR; INVENTORY; ADULTS; BRAIN; HYPERSOCIABILITY; VULNERABILITY; INDIVIDUALS;
D O I
10.1016/j.ridd.2014.06.010
中图分类号
G76 [特殊教育];
学科分类号
040109 ;
摘要
Williams syndrome (WS) is a neurogenetic disorder known for its "hypersocial" phenotype and a complex profile of anxieties. The anxieties are poorly understood specifically in relation to the social-emotional and cognitive profiles. To address this gap, we employed a Wechsler intelligence test, the Brief Symptom Inventory, Beck Anxiety Inventory, and Salk Institute Sociability Questionnaire, to (1) examine how anxiety symptoms distinguish individuals with WS from typically developing (TD) individuals; and (2) assess the associations between three key phenotypic features of WS: intellectual impairment, social-emotional functioning, and anxiety. The results highlighted intensified neurophysiological symptoms and subjective experiences of anxiety in WS. Moreover, whereas higher cognitive ability was positively associated with anxiety in WS, the opposite pattern characterized the TD individuals. This study provides novel insight into how the three core phenotypic features associate/dissociate in WS, specifically in terms of the contribution of cognitive and emotional functioning to anxiety symptoms. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2403 / 2415
页数:13
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