肢带型肌营养不良症初始由 Walton 所描述,在1967年被认作为一种单独的临床疾病。有关该病的临床、遗传和变异性的报告已有发表,作者在本文报告1例可逆的病例。病例报告患者36岁,男性,为作遗传咨询而就诊,在家四兄弟中排行第3,10岁前的生长发育正常,10岁开始感觉腿和腰带肌无力。3年后神经病学家检查发现肩胛、腰带和大腿有严重的肌肉萎缩,有腰部脊柱前凸和双侧翼状肩胛,不使用双手时不能从仰卧位 Muscular dystrophy, originally described by Walton, was considered a separate clinical disease in 1967. A report on the clinical, genetic and variability of the disease has been published and the authors report 1 reversible case in this article. Case Report A 36-year-old man, male, referred for genetic counseling, ranks third in the family of four brothers and grows well before the age of 10 and begins to feel leg and girdle weakness at 10 years of age. Neuropathic examination three years later revealed severe muscular atrophy on the shoulder blades, waist band and thighs, lumbar lordosis and bilateral winged shoulder blades,