AUTISM AND MITOCHONDRIAL DISEASE

被引:77
作者
Haas, Richard H. [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Neurosci, UCSD Mitochondrial & Metab Dis Ctr, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pediat, UCSD Mitochondrial & Metab Dis Ctr, La Jolla, CA 92093 USA
关键词
autism spectrum disorder; mitochondrial disease; mitochondria; genetics; copy number variation; immune modulators; PERVASIVE DEVELOPMENTAL DISORDERS; CHRONIC INTESTINAL PSEUDOOBSTRUCTION; SPECTRUM DISORDERS; GASTROINTESTINAL SYMPTOMS; INFANTILE-AUTISM; COPY-NUMBER; NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY; DIAGNOSTIC-CRITERIA; IMMUNE ACTIVATION; CHILDREN;
D O I
10.1002/ddrr.112
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Autism spectrum disorder (ASD) as defined by the revised Diagnostic and Statistical Manual of Mental Disorders: DSM IVTR criteria (American Psychiatric Association [2000] Washington, DC: American Psychiatric Publishing) as impairment before the age of 3 in language development and socialization with the development of repetitive behaviors, appears to be increased in incidence and prevalence. Similarly, mitochondrial disorders are increasingly recognized. Although overlap between these disorders is to be expected, accumulating clinical, genetic, and biochemical evidence suggests that mitochondria! dysfunction in ASD is more commonly seen than expected. Some patients with ASD phenotypes clearly have genetic-based primary mitochondrial disease. This review will examine the data linking autism and mitochondria. (C) 2010 Wiley-Liss, Inc. Dev Disabil Res Rev 2010;16:144-153.
引用
收藏
页码:144 / 153
页数:10
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