Autism in Dravet syndrome: Prevalence, features, and relationship to the clinical characteristics of epilepsy and mental retardation

被引:91
作者
Li, Bing-Mei
Liu, Xiao-Rong
Yi, Yong-Hong
Deng, Yu-Hong
Su, Tao
Zou, Xin
Liao, Wei-Ping [1 ]
机构
[1] Guangzhou Med Univ, Inst Neurosci, Guangzhou 510260, Guangdong, Peoples R China
关键词
Autism; Dravet syndrome; Epilepsy; Seizure; Mental retardation; SEVERE MYOCLONIC EPILEPSY; DISORDERS; SPECTRUM; CHILDREN;
D O I
10.1016/j.yebeh.2011.04.060
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Autism is a pervasive developmental disorder that frequently co-occurs with epilepsy. Dravet syndrome is a severe epileptic encephalopathy associated with psychomotor developmental delay. Autism in Dravet syndrome, however, has rarely been studied. In this study, the prevalence and features of autism in patients with Dravet syndrome, their potential association with mental retardation, and the clinical characteristics of epilepsy were investigated. Clinical data of 37 patients with Dravet syndrome were collected, and evaluations of autism and mental retardation were performed. Nine patients (24.3%) met the criteria for autism. All patients with autism showed speech delay, no emotional reciprocity, and narrow interests, whereas 89.3, 46.4, and 39.9% of patients without autism had speech delay, short temper, and narrow interests, respectively. Mental retardation was observed in 94.6% of patients with Dravet syndrome, with more frequent severe or profound mental retardation in those with autism. The clinical features of epilepsy did not statistically differ between the patients with autism and the patients without autism. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:291 / 295
页数:5
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