Epilepsy, autism, and neurodevelopment: Kindling a shared vulnerability?

被引:27
作者
Gilby, Krista L. [1 ]
O'Brien, Terence J. [1 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Parkville, Vic 3052, Australia
关键词
Epilepsy; Autism spectrum disorder; Neurodevelopment; Comorbidity; RESISTANT SLOW RATS; EPILEPTIFORM EEG ABNORMALITIES; SPECTRUM DISORDERS; SEIZURE-PRONE; RETT-SYNDROME; EL MICE; STRAINS; MODEL; MOUSE; PHENOTYPES;
D O I
10.1016/j.yebeh.2012.11.002
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
Epilepsy and autism spectrum disorder (ASD) share many primary and comorbid symptoms. The degree of clinical overlap is believed to signify a 'spectrum of vulnerability' that arises out of an early common dysfunction in central nervous system development. However, research into the underlying, and potentially shared, etiopathological mechanisms is challenging given the extensive comorbidity profiles. Adding to the degree of difficulty is the frequently evolving recompartmentalization of diagnostic criteria within each disorder. This review discusses potential preclinical strategies that, through the use of animal models, are designed to gain insight into the biological basis of the overlap between epilepsy and autism and to foster a rapid clinical translation of the insights gained. This article is part of a Special Issue entitled "The Future of Translational Epilepsy Research". (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:370 / 374
页数:5
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