HEREDITARY PAROXYSMAL ATAXIA WITH NEUROMYOTONIA

被引：23

作者：

VAAMONDE, J ^{[1
]}

ARTIEDA, J ^{[1
]}

OBESO, JA ^{[1
]}

机构：

[1] CLIN UNIV PAMPLONA,DEPT NEUROL,MOVEMENT DISORDERS UNIT,APDO 192,E-31080 PAMPLONA,SPAIN

来源：

MOVEMENT DISORDERS | 1991年 / 6卷 / 02期

关键词：

Neuromyotonia; Paroxysmal ataxia;

D O I：

10.1002/mds.870060218

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

The clinical manifestations of a patient with hereditary paroxysmal ataxia and neuromyotonia are described. Generalized tremor, triggered by sudden movements, and spasms of hand and foot muscles were the main clinical findings. Electromyogram (EMG) and nerve blocking studies led to the diagnosis of neuromyotonia. Treatment with acetozolamide was of no therapeutic value, confirming previous observations about the difference in response of paroxysmal ataxia with and without neuromyotonia.

引用

页码：180 / 182

页数：3

共 8 条

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