作者报告一例常染色体显性遗传性疾病,表现为慢性进行性肱骨骨盆肌无力和心肌病.这种病类似性—连锁性肌营养不良中的Emery-Dreifuss型,但遗传方式和肌无力的分布有所不同.病例报告:患者男性,39岁,因自儿童时开始进行性无力就诊.10岁时发现轻度胸腰椎弯曲和双跟腱缩短,诊断为进行性肌营养不良, The authors report an autosomal dominant inherited disorder characterized by chronic progressive humeral pelvic muscle weakness and cardiomyopathy, a disease of the Emery-Dreifuss type that is a hallmark of synchronous muscle dystrophy but a mode of inheritance and myasthenia gravis A case report: Male patient, age 39, was diagnosed with progressive muscular dystrophy due to mild thoracolumbar flexion and double Achilles tendon shortening at age 10,