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Towards the neural basis for hypersociability in a genetic syndrome.

作者信息

Bellugi U, Adolphs R, Cassady C, Chiles M

机构信息

Laboratory for Cognitive Neuroscience, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.

出版信息

Neuroreport. 1999 Jun 3;10(8):1653-7. doi: 10.1097/00001756-199906030-00006.

DOI:10.1097/00001756-199906030-00006
PMID:10501552
Abstract

Williams syndrome (WMS), a rare disorder with a distinctive profile of medical, psychological, neurophysiological and neuroanatomical characteristics, results from hemizygous deletion of about 20 genes. The phenotype exhibits specific dissociations in higher cognitive functions: general cognitive deficits but spared linguistic abilities; extreme spatial cognitive deficits, but intact face processing. Of special interest is an unusual social phenotype in WMS: an overly friendly, engaging personality and excessive sociability with strangers. In this first experimental study of social behavior in WMS, we report that WMS subjects show an abnormal positive bias in their social judgments of unfamiliar individuals, consistent with their behavior in real life. Our findings contribute to an understanding of the neural and genetic bases of human social behavior.

摘要

相似文献

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Towards the neural basis for hypersociability in a genetic syndrome.
Neuroreport. 1999 Jun 3;10(8):1653-7. doi: 10.1097/00001756-199906030-00006.
2
Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome.连接认知、大脑与分子遗传学:来自威廉姆斯综合征的证据。
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II. Hypersociability in Williams Syndrome.二、威廉姆斯综合征中的过度社交性。
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"Everybody in the world is my friend" hypersociability in young children with Williams syndrome.患有威廉姆斯综合征的幼儿的“世界上每个人都是我的朋友”式高度社交性。
Am J Med Genet A. 2004 Jan 30;124A(3):263-73. doi: 10.1002/ajmg.a.20416.
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VI. Genome structure and cognitive map of Williams syndrome.六、威廉姆斯综合征的基因组结构与认知图谱
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I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses.一、威廉姆斯综合征的神经认知特征:优势与劣势并存的复杂模式。
J Cogn Neurosci. 2000;12 Suppl 1:7-29. doi: 10.1162/089892900561959.
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Affiliative behavior in Williams syndrome: social perception and real-life social behavior.Williams 综合征的亲和行为:社会知觉和现实生活中的社会行为。
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Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.GTF2I 基因部分缺失导致威廉姆斯综合征,会增加社会互动。
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Williams syndrome hypersociability: a neuropsychological study of the amygdala and prefrontal cortex hypotheses.威廉斯综合征过度社交能力:杏仁核和前额叶皮质假说的神经心理学研究。
Res Dev Disabil. 2011 May-Jun;32(3):1169-79. doi: 10.1016/j.ridd.2011.01.006. Epub 2011 Feb 12.

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Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndrome.与威廉姆斯-贝伦综合征非典型缺失相关的社会、神经发育、内分泌和头围大小差异。
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Explicit Oral Narrative Intervention for Students with Williams Syndrome.针对威廉姆斯综合征学生的明确口头叙事干预
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