Tachi N, Sasaki K, Yamada T, Imamura S, Mike T
Department of Pediatrics, Sapporo Medical College, Japan.
Pediatr Neurol. 1990 Jan-Feb;6(1):54-6. doi: 10.1016/0887-8994(90)90080-k.
Dystrophin is the gene product affected in Duchenne muscular dystrophy (DMD). Dystrophin is demonstrably absent with immunocytochemical staining and undetectable by western blotting of DMD muscles. We report an isolated 7-year-old girl with DMD. Analysis of the patient's and her mother's DNA, with probes covering the DMD gene, disclosed no deletion. We have studied dystrophin in biopsied muscle from the patient using antidystrophin antibody in combination with immunofluorescence. Random presence of normal and dystrophin-deficient fibers were indicative of mosaic expression. Dystrophin immunocytochemistry may be useful for accurate diagnosis of affected females.
肌营养不良蛋白是杜氏肌营养不良症(DMD)中受影响的基因产物。通过免疫细胞化学染色可明显看出DMD肌肉中缺乏肌营养不良蛋白,且在蛋白质印迹法检测中无法检测到。我们报告了一名患有DMD的7岁孤立女童。用覆盖DMD基因的探针分析患者及其母亲的DNA,未发现缺失。我们使用抗肌营养不良蛋白抗体结合免疫荧光技术研究了患者活检肌肉中的肌营养不良蛋白。正常纤维和缺乏肌营养不良蛋白的纤维随机出现表明存在嵌合表达。肌营养不良蛋白免疫细胞化学可能有助于准确诊断患病女性。