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无近端萎缩的X连锁脊髓和延髓性肌萎缩

X-linked spinal and bulbar muscular atrophy without proximal atrophy.

作者信息

Boz Cavit, Sahin Nilufer, Kalay Ersan, Velioglu Sibel, Ozmenoglu Mehmet

机构信息

Department of Neurology, Medical Faculty of Karadeniz Technical University, 61080 Trabzon, Turkey.

出版信息

Clin Neurol Neurosurg. 2002 Dec;105(1):14-7. doi: 10.1016/s0303-8467(02)00055-0.

Abstract

We report on a case of genetically proven X-linked spinal and bulbar muscular atrophy (X-SBMA) with prominent distal muscle atrophy and without proximal muscle involvement. The patient was a 35-year-old man who had a history of slow progressive hand and distal leg muscle weakness and wasting for 10 years. Motor nerve conduction velocities were normal with reduced compound muscle action potential amplitudes of hand and foot muscles. Sensory action potential amplitudes were small. Needle EMG revealed a chronic partial denervation with reduced interference in hand and distal leg muscles but with normal heading in all tested proximal muscles. Genetic studied showed an expansion of CAG repeat in the first exon of the androgen receptor gene, which suggests diagnosis of X-SBMA. The importance of genetic studies in this patient with unusual clinical presentation is emphasized.

摘要

我们报告一例经基因证实的X连锁脊髓和延髓性肌萎缩(X-SBMA),其具有明显的远端肌肉萎缩且无近端肌肉受累。患者为一名35岁男性,有10年缓慢进展的手部和远端腿部肌肉无力及萎缩病史。运动神经传导速度正常,但手部和足部肌肉复合肌肉动作电位幅度降低。感觉动作电位幅度较小。针极肌电图显示手部和远端腿部肌肉有慢性部分失神经,干扰减少,但所有测试的近端肌肉均正常。基因研究显示雄激素受体基因第一外显子中的CAG重复序列扩增,这提示X-SBMA的诊断。强调了基因研究在该临床表现不典型患者中的重要性。

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