可能的肯尼迪病模拟平山病:1例报告

Soo-Im Jang, Soo-Hyun Park, Seul-Gi Choi, Sae-Nal Lee, Jiyoung An, Nam-Hee Kim
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引用次数: 0

摘要

脊髓和球性肌萎缩症(Kennedy病)是一种x连锁的、成人发病的运动神经元疾病,其特征是缓慢、进行性的球和四肢肌肉无力,雄激素受体基因中CAG三联体重复扩增。平山病(HD)的特点是青少年发病时不对称无力和手部肌萎缩,在亚洲男性中最常见。我们报告一个非典型肯尼迪病的病人,表现为不对称的手部无力和HD的典型萎缩。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Probable Kennedy Disease Mimicking Hirayama Disease: A Case Report
Spinal and bulbar muscular atrophy (Kennedy disease) is an X-linked, adult-onset motor neuron disease characterized by slow, progressive weakness of the bulbar and extremity muscles with CAG triplet repeat expansion in the androgen receptor gene. Hirayama disease (HD) is characterized by the juvenile onset of asymmetric weakness and amyotrophy of the hand and is most common in males in Asia. We report a patient with atypical Kennedy disease presenting with asymmetric hand weakness and atrophy typical of HD.
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