儿童期起病的眼阵挛-肌阵挛-共济失调41年随访：小脑萎缩、多相性复发及对静脉注射免疫球蛋白的反应

Forty-one year follow-up of childhood-onset opsoclonus-myoclonus-ataxia: cerebellar atrophy, multiphasic relapses, and response to IVIG.

作者信息

Pranzatelli Michael R, Tate Elizabeth D, Kinsbourne Marcel, Caviness Verne S, Mishra Bibhuti

机构信息

The National Pediatric Myoclonus Center, Departments of Neurology and Pediatrics, Southern Illinois University School of Medicine, Springfield, Illinois 62702, USA.

出版信息

Mov Disord. 2002 Nov;17(6):1387-90. doi: 10.1002/mds.10283.

DOI:10.1002/mds.10283

PMID:12465092

Abstract

We report on an adult with opsoclonus-myoclonus-ataxia syndrome experiencing widely spaced neurological relapses, who was followed for 41 years. His responses to treatment are described.

摘要

我们报告了一例患有眼阵挛-肌阵挛-共济失调综合征的成年人，其神经功能复发间隔时间较长，随访了41年。描述了他对治疗的反应。