{"title":"[Diagnosis and treatment of Angelman syndrome].","authors":"X N Du, J Wang, Y Wang","doi":"10.3760/cma.j.cn112140-20230322-00198","DOIUrl":null,"url":null,"abstract":"Angelman综合征是由于母源染色体15q11.2-q13区域UBE3A基因功能缺陷所导致的基因组印记遗传病。临床上表现为严重神经发育障碍，包括智力障碍、语言缺失、癫痫发作及异常的脑电发放、运动障碍、睡眠及喂养问题、特殊面容及特异的行为特征。.","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":"61 7","pages":"667-669"},"PeriodicalIF":0.0000,"publicationDate":"2023-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhonghua er ke za zhi = Chinese journal of pediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3760/cma.j.cn112140-20230322-00198","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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