假肥大型进行性肌营养不良症,又称Duchenne型,属于X伴性隐性遗传,男性发病,女性为异常基因携带者而不发病。作者诊治过3例女性假肥大型肌营养不良症,现报告如下。病例报告例1,张某,女,30岁,未婚,患者大约10岁时,在学校上体育课,双腿跑步无力。一年后不能跑步。在当地医院按“风湿症”治疗,不见好转,走路无力,上身摇摆,脚尖触地,不能上楼。几年后双上肢 Duchenne muscular dystrophy, also known as Duchenne type, belongs to the X-associated recessive inheritance, male onset, women with abnormal gene carriers without disease. The author diagnosed 3 cases of female Duchenne muscular dystrophy, are as follows. Case report 1, Zhang, female, 30 years old, unmarried, about 10 years of age, physical education in school, legs running weakness. Can not run after one year. In the local hospital by “rheumatism” treatment, no improvement, walking weak, upper body swing, toe touch, can not go upstairs. A few years later, both upper extremities