发育医学电子杂志 2022, Vol. 10 Issue (6): 453-455 DOI: 10.3969/j.issn.2095-5340.2022.06.009 |
临床遗传
病例报告
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SCN2A 基因相关新生儿期癫痫 1 例并
文献复习 |
高源 高金枝 徐三清 陈玲 |
1. 湖北省第三人民医院 新生儿科,湖北
武汉 430000;2. 华中科技大学同济医学院附属同济医院 新生儿科,湖北 武汉
430000 |
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SCN2A gene related neonatal seizures: one case reportand literature review
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Gao Yuan, Gao Jinzhi, Xu Sanqing, et al |
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摘要 患儿,男,生后18 d,因“反复抽搐16 d”于
2020年9月就诊于华中科技大学同济医学院附属同济
医院新生儿科门诊。患儿系第1胎第1产,因“脐带
绕颈3周”剖宫产娩出,出生体质量3.2 kg,围产期
无窒息缺氧史。母亲孕期无特殊病史。家族中无类
似病史。患儿生后第3天无明显诱因出现抽搐,仅表
现为四肢抖动,持续数秒后缓解,2~3 h发作1次(均
为吃奶时发现)。当天于外院住院治疗,予苯巴比
妥治疗8 d。1周后再次惊厥发作,表现为四肢抽动、
双手握拳、伴咂嘴、眨眼、双眼凝视,起初3~4 h发
作1次,逐渐转为1~2 h发作1次,且发作期延长,原持
续数秒至半分钟后缓解,后持续约半分钟至1 min才可
缓解。遂转至我院。
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关键词:
癫痫
新生儿
突变
SCN2A
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收稿日期: 2021-05-06
发布日期: 2022-11-30
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基金资助: 国家自然科学基金青年项目(82001601) |
通讯作者:
高金枝
E-mail: gjz_5460@126.com
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