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先天性挛缩性细长指(趾)症一例

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摘要 患儿:女,15岁。主诉发现脊柱畸形7年余。该患儿G1P1,足月顺产,出生后无窒息抢救史,出生体重2600g。母亲孕期有在高磁场环境工作史。患儿运动发育落后,1岁抬头,2岁能独坐,3岁能独走。8~9岁时,家长无意中发现胸部左侧骨性突起,随年龄增长逐渐加重,同时出现脊柱后弯,曾佩戴支具半年,效果不明显。患儿6岁时因先天性心脏病(室间隔缺损)于当地医院行修补术。智力轻度障碍,逻辑思维差。12岁起发现癫痫,长期服用丙戊酸钠控制,否认家族史。检查:可独立行走,行走时轻微跨阈步态,左足外翻。右肩低,左肩高,胸腰椎凸向左侧,背部可见大量浅咖啡色皮肤斑纹,弧度僵硬,棘突无压痛。
作者 冯林
出处 《中华小儿外科杂志》 CSCD 北大核心 2008年第7期448-448,共1页 Chinese Journal of Pediatric Surgery
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参考文献5

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