Saintmard G, Brands G, Debray F-G, Lognard M
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.
Rev Med Liege. 2017 Jul;72(7-8):373-376.
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.
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。
