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新生儿色素失禁症1例

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摘要 色素失禁症(incontinentia pigmenti,IP)又称为Bloch-Sulzberger syndrome,本病较少见,临床上发现该病多发于新生儿期,该病属于X染色体连锁显性遗传性疾病,新生儿期患儿多表现为皮肤损害,临床上常被误诊为感染性脓疱疹、严重湿疹、大疱表皮松解症等疾病,常被误诊而延误诊断,该病常可引起中枢神经系统损害,可能导致生长发育迟缓及眼、毛发、牙齿等处的发育异常,故应提高对该病的认识,做到早诊断、早治疗.收治新生儿色素失禁症患儿1例,报告如下.
出处 《中国社区医师(医学专业)》 2012年第20期268-268,共1页
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