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PARS2基因变异致早发性婴儿癫痫性脑病1例报告
引用本文:王秀英,田杨,石真,侯池,李小晶,朱海霞,曹彬彬,陈文雄,伍湘玲.PARS2基因变异致早发性婴儿癫痫性脑病1例报告[J].临床儿科杂志,2022,40(4):306-310.
作者姓名:王秀英  田杨  石真  侯池  李小晶  朱海霞  曹彬彬  陈文雄  伍湘玲
作者单位:广州市妇女儿童医疗中心神经内科(广东广州 510000)
摘    要:遗传学因素是早发性婴儿癫痫性脑病的常见病因.文章鉴定1例早发性婴儿癫痫性脑病患儿的致病性变异.男性患儿,4月27日龄,反复抽搐发作20余天,表现为痉挛发作,伴发育迟缓.其父母表型无异常.患儿存在PARS 2基因c.287 G>A(p.Arg 96 His)和c.283 G>A(p.Val 95 Ile)复合杂合变异,前...

关 键 词:PARS2基因  癫痫  脑病  婴儿
收稿时间:2021-05-17

Early infantile-onset epileptic encephalopathy caused by PARS2 gene variation: a case report
WANG Xiuying,TIAN Yang,SHI Zhen,HOU Chi,LI Xiaojing,ZHU Haixia,CAO Binbin,CHEN Wenxiong,WU Xiangling.Early infantile-onset epileptic encephalopathy caused by PARS2 gene variation: a case report[J].The Journal of Clinical Pediatrics,2022,40(4):306-310.
Authors:WANG Xiuying  TIAN Yang  SHI Zhen  HOU Chi  LI Xiaojing  ZHU Haixia  CAO Binbin  CHEN Wenxiong  WU Xiangling
Institution:Neurology Department, Guangzhou Women and Children’s Medical Center, Guangzhou 510000, Guangdong, China
Abstract:
Keywords:PARS2 gene" target="_blank">PARS2 gene')">PARS2 gene                                                                                                                        epilepsy                                                                                                                        encephalopathy                                                                                                                        infant
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