Merlini L
Muscle Clinic, Istituto Ortopedico Rizzoli, Bologna, Italy.
Neuromuscul Disord. 1994 Jan;4(1):13-5. doi: 10.1016/0960-8966(94)90043-4.
The traditional clinical criteria for identifying a manifesting Duchenne carrier are a positive family history, proximal limb weakness, calf hypertrophy, high serum creatine kinase. We describe a 52-yr-old woman with history of 1 1/2 yr of progressive wasting and weakness of the left calf and marked elevation of serum creatine kinase. Although her quadriceps was clinically silent, it showed mild alterations on ultrasound, computerized tomography and biopsy, and some abnormalities in dystrophin immunostaining, suggesting a manifesting carrier of the dystrophin gene. Given the enormous variability of manifestations of the Duchenne variant in females, we suggest that great care must be exercised in ruling out this genetic disorder.
传统上用于识别症状性杜氏肌营养不良症携带者的临床标准包括家族史阳性、近端肢体无力、小腿肌肉肥大、血清肌酸激酶升高。我们描述了一位52岁女性,有1年半进行性左小腿消瘦和无力病史,血清肌酸激酶显著升高。虽然她的股四头肌在临床上无异常表现,但超声、计算机断层扫描和活检显示有轻度改变,肌营养不良蛋白免疫染色也有一些异常,提示为肌营养不良蛋白基因的症状性携带者。鉴于女性杜氏肌营养不良症变异表现的巨大变异性,我们建议在排除这种遗传疾病时必须格外谨慎。