CAJ | 학술논문

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。
목적보도1례안구진련-기진련종합정병진행문헌복습，이제고대본병적인식화진치수평。방법대1례학진위안구진련-기진련종합정환인적림상자료급치료정황진행총결，병대상관문헌진행복습。결과환인녀，2세，이주로불은、안구급지체진전위주요표현，진단위안구진련-기진련종합정후급여정주인병충구단백、류고순격소치료후병정명현호전。결론안구진련-기진련종합정시일충한견적신경계통자신면역성질병，조기진단치료가개선예후。
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.