[特发性壳核-尾状核萎缩：偏侧肌张力障碍的罕见病因]
[Idiopathic putamino-caudal atrophy: a rare cause of hemidystonia].
作者信息
Korn-Lubetzki I, Reches A
机构信息
Unité Neurologique, Hôpital Bikur Cholim, Jérusalem, Israël.
出版信息
Rev Neurol (Paris). 1994;150(5):359-62.
PMID:7878322
Abstract
Hemidystonia, a rare presentation of dystonia, is usually secondary to various insults of the controlateral basal ganglia. The following report describes hemidystonia which occurred at the age of 16 years. Idiopathic atrophy of the controlateral caudate nucleus and putamen seemed to be the only aetiology.
摘要
偏侧肌张力障碍是肌张力障碍的一种罕见表现，通常继发于对侧基底神经节的各种损伤。以下报告描述了一名16岁时出现的偏侧肌张力障碍患者。对侧尾状核和壳核的特发性萎缩似乎是唯一病因。
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