2016 中国视神经脊髓炎谱系疾病诊断与治疗指南

2016-05-18 中国免疫学会神经免疫分会 中国神经免疫学和神经病学杂志.2016,23(5):155-166.

NMO临床上多以严重的视神经炎(optic neuritis,ON)和纵向延伸的长节段横贯性脊髓炎(longitudinally extensive transverse myelitis,LETM)为特征表现,常于青壮年起病,女性居多,复发率及致残率高。

中文标题:

2016 中国视神经脊髓炎谱系疾病诊断与治疗指南

发布日期:

2016-05-18

简要介绍:

视神经脊髓炎(neuromyelitis optica,NMO)是一种免疫介导的以视神经和脊髓受累为主的中枢神经系统(CNS)炎性脱髓鞘疾病。NMO的病因主要与水通道蛋白4抗体(AQP4-IgG)相关,是不同于多发性硬化(multiple sclerosis,MS)的独立疾病实体。


NMO临床上多以严重的视神经炎(optic neuritis,ON)和纵向延伸的长节段横贯性脊髓炎(longitudinally extensive transverse myelitis,LETM)为特征表现,常于青壮年起病,女性居多,复发率及致残率高。

制定者:
中国免疫学会神经免疫学分会
中华医学会神经病学分会神经免疫学组

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2016 中国视神经脊髓炎谱系疾病诊断与治疗指南
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    2021-08-20 医学界有为青年

    学习

    0

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    2017-05-29 海棠胜雪

    好好学习一下

    0

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    2016-11-18 susice

    好好学习下

    0