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首页> 外文期刊>Movement disorders >Palatal tremor, progressive multiple cranial nerve palsies, and cerebellar ataxia: a case report and review of literature of palatal tremors in neurodegenerative disease.
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Palatal tremor, progressive multiple cranial nerve palsies, and cerebellar ataxia: a case report and review of literature of palatal tremors in neurodegenerative disease.

机译:颤,进行性多发性颅神经麻痹和小脑性共济失调:病例报告和神经退行性疾病pa颤的文献复习。

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摘要

We describe a patient with an unusual clinical presentation of progressive multiple cranial nerve palsies, cerebellar ataxia, and palatal tremor (PT) resulting from an unknown etiology. Magnetic resonance imaging showed evidence of hypertrophy of the inferior olivary nuclei, brain stem atrophy, and marked cerebellar atrophy. This combination of progressive multiple cranial nerve palsies, cerebellar ataxia, and PT has never been reported in the literature. We have also reviewed the literature of PT secondary to neurodegenerative causes. In a total of 23 patients, the common causes are sporadic olivopontocerebellar atrophy (OPCA; 22%), Alexander's disease (22%), unknown etiology (43.4%), and occasionally progressive supranuclear palsy (4.3%) and spinocerebellar degeneration (4.3%). Most patients present with progressive cerebellar ataxia and approximately two thirds of them have rhythmic tremors elsewhere. Ear clicks are observed in 13% and evidence of hypertrophy of the inferior olivary nucleus in 25% of the patients. The common neurodegenerative causes of PT are OPCA/multiple system atrophy, Alexander's disease, and, in most of them, the result of an unknown cause.
机译:我们描述了一名病因不明的进展性多发性颅神经麻痹,小脑性共济失调和pa性震颤(PT)的临床表现异常的患者。磁共振成像显示下橄榄核肥大,脑干萎缩和明显的小脑萎缩。进行性多发性颅神经麻痹,小脑性共济失调和PT的这种结合在文献中从未报道过。我们还回顾了继发于神经变性原因的PT的文献。在总共23例患者中,常见原因是偶发性小脑桥小脑萎缩(OPCA; 22%),亚历山大氏病(22%),病因不明(43.4%),偶发性进行性核上性麻痹(4.3%)和脊髓小脑变性(4.3%) )。大多数患者出现进行性小脑性共济失调,其中约三分之二在其他地方有节律性震颤。在13%的患者中观察到耳click声,在25%的患者中发现下橄榄核的肥大迹象。 PT的常见神经退行性病因是OPCA /多系统萎缩,亚历山大氏病,在大多数情况下是未知原因引起的。

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