眼阵挛合并肌阵挛。

J T Holland
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引用次数: 0

摘要

进一步的情况下,光阵挛与肌阵挛的描述。当这种综合征发生在儿童期时,应排除相关的神经母细胞瘤。在所有年龄段的大多数病例中,没有发现潜在的疾病,尽管以前可能有轻微的上呼吸道或胃肠道感染史,这表明可能是脑炎影响脑干机制的原因。一般来说,预后很好,尽管完全恢复可能需要几个月的时间。皮质类固醇和硝西泮可能在治疗有痛苦症状的严重患者中占有一席之地。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Opsoclonus with myoclonus.

A further case of opsoclonus with myoclonus is described. When this syndrome occurs in childhood an associated neuroblastoma should be excluded. In the majority of cases at all ages no underlying disease will be found, although a preceding history of minor upper respiratory or gastrointestinal infection may be elicited, suggesting that a possible encephalitis affecting brain stem mechanisms may be the cause. The prognosis is, as a rule, excellent although full recovery may not occur for many months. Corticosteroids and nitrazepam may have a place in the treatment of severely affected patients with distressing symptoms.

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