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巨头畸形和典型自闭症患者的基因突变:一项系统综述。

gene mutations in patients with macrocephaly and classic autism: A systematic review.

作者信息

Zahedi Abghari Fateme, Moradi Yousef, Akouchekian Mansoureh

机构信息

Department of Medical Genetics and Molecular Biology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Social Determinants of Health Research Center, Kurdistan University of Medical Sciences, Sanandaj, Iran.

出版信息

Med J Islam Repub Iran. 2019 Feb 25;33:10. doi: 10.34171/mjiri.33.10. eCollection 2019.

Abstract

Autism Spectrum Disorder (ASD) is a neurological disorder characterized by massive damage in various fields of development. Impaired social interaction and communication skills, unusual behavior or interests, and repetitive activities are considerably disabling in these patients. There are several challenges in diagnosis of ASD patients such as co-existing epilepsy, difference in clinician attitudes and possibly multifactorial etiology of autistic behavior among children and adults. Research in recent years has emphasized a possible connection between mutations in and macrocephaly (head circumference > 97th centile). Articles in English Language were searched from international databases including Medline (PubMed), Google Scholar, Scopus, and CINHAL from January 1998 to January 2016. The results showed that among 2940 patients with behavioral disorders, 2755 individuals had ASD, and 35 cases with macrocephaly had mutations in . About 77% of the articles (7/9) analyzed mutations in in patients with head circumference more than 2SD away from the mean, but did not check mutations in this gene in other ASD patients without macrocephaly. To the best of our knowledge, this study is the first systematic review on human mutations and classical autistic behavior. We conclude that the presence of macrocephaly may not be sufficient to examine the mutation in this group; however, surveying this gene in all cases of macrocephaly seems to be necessary.

摘要

自闭症谱系障碍(ASD)是一种神经障碍,其特征是在各个发育领域存在大量损害。社交互动和沟通技能受损、行为或兴趣异常以及重复活动在这些患者中具有相当大的致残性。在ASD患者的诊断中存在若干挑战,例如并存癫痫、临床医生态度的差异以及儿童和成人自闭症行为可能的多因素病因。近年来的研究强调了[基因名称]突变与巨头症(头围>第97百分位数)之间可能存在联系。从1998年1月至2016年1月,在包括Medline(PubMed)、谷歌学术、Scopus和CINHAL在内的国际数据库中检索英文文章。结果显示,在2940例行为障碍患者中,2755例患有ASD,35例巨头症患者存在[基因名称]突变。约77%的文章(7/9)分析了头围比平均值高出2个标准差以上的患者中的[基因名称]突变,但未检查其他无巨头症的ASD患者中该基因的突变。据我们所知,本研究是关于人类[基因名称]突变与典型自闭症行为的首次系统综述。我们得出结论,巨头症的存在可能不足以在该组中检测[基因名称]突变;然而,似乎有必要对所有巨头症病例进行该基因的检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82cd/6504940/d8e05b234763/mjiri-33-10-g001.jpg

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