眼球阵挛-肌阵挛综合征1例并文献复习  

Opsoclonus-myoclonus syndrome:a case report and literature review

作　　者：刘京京[1] 王永霞[1] 马秀伟[1] 

机构地区：[1]北京军区总医院附属八一儿童医院神经发育科,北京100700

出　　处：《发育医学电子杂志》2014年第4期234-236,共3页Journal of Developmental Medicine (Electronic Version)

摘　　要：目的报道1例眼球阵挛-肌阵挛综合征并进行文献复习,以提高对本病的认识和诊治水平。方法对1例确诊为眼球阵挛-肌阵挛综合征患儿的临床资料及治疗情况进行总结,并对相关文献进行复习。结果患儿女,2岁,以走路不稳、眼球及肢体震颤为主要表现,诊断为眼球阵挛-肌阵挛综合征后给予静注人丙种球蛋白、类固醇激素治疗后病情明显好转。结论眼球阵挛-肌阵挛综合征是一种罕见的神经系统自身免疫性疾病,早期诊断治疗可改善预后。ObjectiveTo report a case of Opsoclonus-myoclonus syndrome (OMS) and review the related literature to help clinical diagnosis and treatment.Method The clinical data of one OMS child and the related literature were collected and analyzed.Result The child was a two years’ old girl whose principal clinical manifestations were ataxia, opsoclonus and myoclonus. Gamma globulin and steroid were given to the child and was effective.Conclusion OMS is a rare neurological disease. Early diagnosis and treatment can improve prognosis.

关 键 词：眼球阵挛-肌阵挛综合征 儿童 文献复习 

分 类 号：R746[医药卫生—神经病学与精神病学]