[以双下肢进行性肌无力为表现的肢带型肌营养不良症]
[Progressive muscular weakness of lower limbs revealing a limb girdle muscular dystrophy].
作者信息
Saintmard G, Brands G, Debray F-G, Lognard M
机构信息
Service de Médecine Physique et Réadaptation, CHU de Liège, site Sart Tilman, Liège, Belgique.
Service de Médecine Physique et Réadaptation, CHC St Joseph, Liège, Belgique.
出版信息
Rev Med Liege. 2017 Jul;72(7-8):373-376.
PMID:28795552
Abstract
We report the case of a 26-year-old man who initiated a limb girdle muscular dystrophy (lgmd2b). It is a rare and slowly progressive autosomal recessive dysferlinopathy occurring in young adults and for which no treatment is currently known.
摘要
我们报告了一例26岁男性患者，其患有肢带型肌营养不良症（lgmd2b）。这是一种罕见的、进展缓慢的常染色体隐性遗传性dysferlinopathy，发生于年轻人，目前尚无已知的治疗方法。
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