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lin chuang shen jing 1980 nian di 11 qi
Author(s): 
Pages: 29
Year: Issue:  8
Journal: Progress in Japanese Medicine

Keyword:  肾上腺皮质类固醇福山临床症状痉挛磷酸肌酸激酶下肢肌萎缩症先天性脑电图多发肌炎;
Abstract: <正> 本期首先报告了称为福山型先天肌萎缩症的同胞病例。兄为典型的福山型肌萎缩,弟呈Duchenne 型肌萎缩之临床经过,兄15岁5个月,自生后6个月起出现婴儿肌弛缓症状,智能障碍,有痉挛发作,全身关节挛缩,磷酸肌酸激酶中度升高,诊为福山型先天性肌萎缩症。弟8岁5个月,发育尚可。从3岁起走路摇摆,攀登起立,磷酸肌酸激酶极度升高,下肢假肥大,智能发育高度迟延,CT 扫描及脑电图均异常。两者中枢病变无差异,故作者认为弟系良性福山型肌萎缩。木下真男等报告1例先天性多发肌炎。本例最初诊为福山型先天性肌萎缩症,肌活检发现有以细小血管为中心的炎症性肌病改变,投与肾上腺皮质类固醇,血清磷酸肌酸激酶显著下降,临床症状缓慢好转,经4年多观察,确
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