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眼肌型肌营养不良病十分罕见。且极易误诊,国内直至1957年才由张文萃氏进行了首例报告。现将作者经历的3例报告如下。例1 曹××男21岁1岁时发现双眼睁开困难,复视。症状越来越严重,早晚无轻重差别,休息后症状也不减轻。于某医院诊断为肌无力症,曾注射新斯的明多次,毫不见效。饮食无呛咳,说话声音正常。否认家族史。周身一般状况佳,意识清,检查时合作。双上睑下垂,用力睁眼时,睑裂约2mm。双瞳孔等大,光反射及调节反射均敏感。双眼球固定在正中位,各方向运动不能。软腭运动正常,咽反射正常。运
Ocular muscular dystrophy is very rare. And easily misdiagnosed, domestic only by 1957 Zhang Wenchuang conducted the first report. Now the author experienced three cases are as follows. Example 1 Cao × × male 21 years old 1 year old found his eyes open difficulties, diplopia. More and more serious symptoms, no difference between morning and evening, the symptoms did not reduce after the rest. Diagnosed with myasthenia in a hospital, once injected neostigmine many times, no effect. No choking diet, speak properly. Denied family history. Good general condition of the whole body, awareness, inspection cooperation. Double ptosis, forced eyes open, blepharophimosis about 2mm. Double pupil and other large, light reflection and adjust the reflection are sensitive. Eyes fixed in the median, all directions can not exercise. Soft palate movement is normal, normal pharyngeal reflex. Shipped