Hyperammonemia presenting as opsoclonus–myoclonus–ataxia–tremor syndrome: A case report

Q3 Medicine
S. Manorenj, G. Verma
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引用次数: 0

Abstract

Opsoclonus myoclonus syndrome (OMS) is a rare autoimmune condition occurring due to Purkinje cell degeneration due to remote aetiology. Most often it occurs as a paraneoplastic syndrome. Here we report a case of opsoclonus-myoclonus–ataxia tremor syndrome in a 60-year-old woman that occurred due to hyperammonemia and she recovered completely with immunotherapy and correction of hyperammonemia. OMS is the first in literature associated with hyperammonemia.
高氨血症表现为视锁肌-肌阵挛-共济失调-震颤综合征:一例报告
肌阵挛综合征(OMS)是一种罕见的自身免疫性疾病,由病因遥远的浦肯野细胞变性引起。最常见的是作为副肿瘤综合征出现。在这里,我们报告了一例60岁女性的视锁肌痉挛-共济失调震颤综合征,该综合征发生于高氨血症,通过免疫治疗和高氨血症矫正,她完全康复。OMS是第一个与高氨血症相关的文献。
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来源期刊
Annals of Movement Disorders
Annals of Movement Disorders Medicine-Surgery
CiteScore
0.60
自引率
0.00%
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0
审稿时长
17 weeks
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