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[1]魏春苗,夏桂枝,任榕娜.伴强直发作的Dravet综合征2例报告并文献复习[J].医学研究与战创伤救治(原医学研究生学报),2018,20(02):152-155.[doi:10.3969/j.issn.1672-271X.2018.02.010]
　WEI Chun-miao,XIA Gui-zhi,REN Rong-na.Dravet syndrome with tonic seizure: 2 cases report and literature review[J].JOURNAL OF MEDICALRESEARCH —COMBAT TRAUMA CARE,2018,20(02):152-155.[doi:10.3969/j.issn.1672-271X.2018.02.010]
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伴强直发作的Dravet综合征2例报告并文献复习()
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《医学研究与战创伤救治》（原医学研究生学报）[ISSN:1672-271X/CN:32-1713/R]

卷:
第20卷
期数:
2018年02期
页码:
152-155
栏目:
出版日期:
2018-03-20

文章信息/Info

Title:
Dravet syndrome with tonic seizure: 2 cases report and literature review
作者:
魏春苗; 夏桂枝; 任榕娜
作者单位：350025 福州，蚌埠医学院福总教学医院儿科（魏春苗）；350025 福州，福建医科大学福总临床医学院儿科（夏桂枝）；350025 福州，南京军区福州总医院儿科（任榕娜）
Author(s):
WEI Chun-miao1;  XIA Gui-zhi2;  REN Rong-na3
(1.Department of Paediatic，Fuzhou General Hospital Clinical Medical College of Bengbu Medical University, Fuzhou 350025,Fujian,China;2. Department of Paediatic，Fuzhou General Hospital Clinical Medical College of Fujian Medical University, Fuzhou 350025, F
关键词:
Dravet综合征; 强直发作; SCN1A基因; 新发突变
Keywords:
Dravet syndrome;  tonic seizure;  SCN1A gene;  de novo mutation
分类号:
R725
DOI:
10.3969/j.issn.1672-271X.2018.02.010
文献标志码:
A
摘要:
目的 分析伴强直发作的Dravet综合征的临床及基因突变特点，以期对Dravet综合征少见表型早期诊断及合理治疗。方法 对2011年1月至2017年3月在福州总医院儿科神经专科门诊及病房诊治的2例伴强直发作的Dravet综合征的临床和基因突变特点进行回顾性分析，结合相关文献进行总结。结果 2例患儿分别在出生5个月和8个月时以热性惊厥起病,病程中除有全身及偏侧阵挛、强直阵挛和不典型失神等多种Dravet综合征常见的发作形式外，均出现了Dravet综合征少见的强直发作，2例患儿均对多种抗癫痫药物疗效不佳，现均有不同程度的精神运动发育落后,2例基因检测均为SCN1A基因新发错义突变。结论 Dravet综合征可出现少见的强直发作形式，基因检测有助于这种Dravet综合征少见表型的早期诊断及合理治疗。
Abstract:
Objective To achieve early diagnosis and correct treatment to the rare phenotype of Dravet syndrome to analyze the clinical features and genetic mutation of Dravet syndrome with tonic seizure.Methods The clinical information was collected from Fuzhou General Hospital between January 2011 to March 2017. The related literature were reviewed. Results Febrile seizures onset in the 5th month and the 8th month after birth for 2 cases. Except for general clonic, hemiclonic, general tonic-clonic, myoclonus and atypical absence seizure, tonic seizure was also observed in the course of the disease and the children represented slowing of psychomotor development. De novo missense mutation of SCN1A gene was found by Genetic screening for 2 cases.Conclusion Tonic seizure can be observed on the Dravet syndrome. Genetic screening is helpful to early diagnosis and correct treatment for this rare phenotype.

参考文献/References:

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更新日期/Last Update: 2018-03-20