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患者 男性,62岁,工人。以肌无力、肢体肌肉萎缩,发音障碍并进行性加重4年,于1994年10月5日入院。患者于1990年1月感到双下肢无力,两年后发展到四肢无力,双下肢及双手肌肉萎缩,腰部及两大腿肌肉出现跳动,最近半年出现发音不清,但无喝水呛咳及吞咽困难。1994年5月经中国医科大学诊断为进行性脊髓性肌萎缩,并经住院中西医结合治疗2个月,无明显疗效。既往无家族遗传病史。检查:T 36.8℃,P 84次
Male patient, 62 years old, worker. Myasthenia, limb muscle atrophy, dysphonia and progressive aggravating 4 years, admitted to hospital on October 5, 1994. Patients felt weakness in both lower extremities in January 1990, development of weakness in both arms after two years, muscle weakness in both lower extremities and both hands, and beating of muscles in the waist and the two thighs. In the last six months, there was unclear articulation, but no cough and dysphagia in drinking water . May 1994 by the China Medical University diagnosis of progressive spinal muscular atrophy and hospitalized by Integrative Medicine for 2 months, no significant effect. No past family history of genetic disease. Check: T 36.8 ℃, P 84 times