良性X连锁肌营养不良（贝克型）：一个进展非常缓慢的家系。
Benign X-linked muscular dystrophy (Becker type): a kindred with very slow rate of progression.
作者信息
Kloster R
出版信息
Acta Neurol Scand. 1983 Nov;68(5):344-9. doi: 10.1111/j.1600-0404.1983.tb04842.x.
Abstract
A family with benign X-linked muscular dystrophy (Becker type) has been studied. There was a total of 8 affected males, 7 of whom were alive. The clinical and pathological features are presented. The clinical symptoms started in the 2nd decade for most of the patients. The rate of progression was very slow and 3 patients became confined to a wheelchair in the second half of the 6th decade.
摘要
对一个患有良性X连锁肌营养不良（贝克型）的家族进行了研究。共有8名受影响男性，其中7人存活。文中呈现了其临床和病理特征。大多数患者的临床症状始于第二个十年。疾病进展非常缓慢，60岁后半期有3名患者只能依靠轮椅行动。
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