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大田原综合征一例 被引量:2

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摘要 患儿男,3个月10 d,因反复抽搐10 d入院.入院前10d无明显诱因开始出现抽搐,表现为双眼眨动、口角抽动、四肢痉挛发作,每次持续数秒至十余秒,可自然缓解,成串发作,每串10余次,每天6~7串.患儿系第2胎第2产,足月顺产,出生体重3 500 9,否认出生窒息史.母孕产史无异常,否认家族癫痫史及遗传病史.
出处 《中华儿科杂志》 CAS CSCD 北大核心 2015年第4期304-305,共2页 Chinese Journal of Pediatrics
基金 国家自然科学基金(81370771)
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参考文献12

  • 1Ohtahara S, Yamatogi Y. Epileptic encephalopathies in early infancy with suppression-burst [ J ]. J Clin Neurophysiol, 2003,20 (6) :398-407.
  • 2杨群,邵肖梅,朱珍.半侧巨脑畸形导致大田原综合征一例[J].中华儿科杂志,2008,46(2):93-93. 被引量:1
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二级参考文献2

  • 1Ohtahara S, Yamatogi Y. Epileptic encephalopalhies in early infancy with suppression-bursl. J Clin Neurophysiol, 2003, 20: 398-407.
  • 2Salamon N. Andres M, Chute DJ. et al. Contrateral hemimicrencephaly and clinicalpathological correlations in children with hemimegalencephaly. Brain, 2006, 129: 352-365.

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