{"title":"[A case of haploinsufficiency of A20 caused by new variation of TNFAIP3 gene].","authors":"F M Xue, C Liu, Z Lei, C An","doi":"10.3760/cma.j.cn112140-20230202-00072","DOIUrl":null,"url":null,"abstract":"患儿 女，5岁，因“间断发热、腹痛、腹泻2个月余”就诊于郑州大学附属儿童医院，结肠镜检查发现全结肠出现多处不规则深溃疡，肛周可见脓肿。基因检测显示患儿存在TNFAIP3基因杂合变异（NM_001270508：c.866delA），而其父母均为野生型。患儿确诊A20单倍体不足，予营养支持、沙利度胺口服治疗，后因严重胃肠道反应停用沙利度胺，给予生物制剂抗肿瘤坏死因子-α制剂（英夫利昔单抗）治疗半年余，病情得到有效控制。.","PeriodicalId":23998,"journal":{"name":"Zhonghua er ke za zhi = Chinese journal of pediatrics","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-08-02","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.cn112140-20230202-00072","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
京公网安备 11010802042870号
京ICP备2023020795号-1
分享
求助内容：
应助结果提醒方式：
扫码关注我们
