最近报道一个Duchennc肌营养不良的家族,受累兄长的生长激素缺陷,其病情明显地比弟弟轻。根据上述观察,作者对9例Duchenne肌营养不良患儿使用生长激素抑制剂进行了治疗。患儿是由典型的临床病程和身体特征而确诊的,其诊断标准包括骨盆股骨无力,腓肠肌假性肥大,患儿家族史,血清肌酸激酶(CK)、乳酸脱氢酶(LDH)、谷草转氨酶(SGOT)水平升 A recent Duchennc muscular dystrophy family, reported to have a growth hormone deficiency in his elder brother, was significantly less severe than his younger brother. Based on the above observations, the authors treated nine patients with Duchenne muscular dystrophy with growth hormone inhibitors. Children are diagnosed with typical clinical course and physical characteristics. Diagnostic criteria include pelvic femur weakness, gastrocnemius pseudo-hypertrophy, pediatric family history, serum creatine kinase (CK), lactate dehydrogenase (LDH), aspartate Aminotransferase (SGOT) level rise