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继发于生物蝶呤合成缺陷的阵发性震颤和口面部运动障碍。

Paroxysmal tremor and orofacial dyskinesia secondary to a biopterin synthesis defect.

作者信息

Factor S A, Coni R J, Cowger M, Rosenblum E L

机构信息

Department of Neurology, Albany Medical College, NY 12208.

出版信息

Neurology. 1991 Jun;41(6):930-2. doi: 10.1212/wnl.41.6.930.

Abstract

We report a child with a systemic biopterin synthesis defect due to an absence of 6-pyruvoyl-tetrahydropterin synthase who had an unusual presentation, with three episodes of coarse "rubral-like" tremor in arms and legs orofacial dyskinesia between the ages of 3 and 6 months. Response to levodopa therapy and CSF neurotransmitter metabolite concentrations before and after therapy suggests that his clinical syndrome resulted from a secondary dopamine deficiency.

摘要

我们报告了一名因缺乏6-丙酮酰四氢生物蝶呤合酶而患有全身性生物蝶呤合成缺陷的儿童,该患儿有不寻常的表现,在3至6个月大时出现了三次手臂和腿部的粗大“红核样”震颤发作以及口面部运动障碍。左旋多巴治疗的反应以及治疗前后脑脊液神经递质代谢物浓度表明,他的临床综合征是由继发性多巴胺缺乏引起的。

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