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Adams-Oliver Syndrome: A Case with Full Expression

机译:亚当斯-奥利弗综合征:一个完整​​表达的案例

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摘要

Adams-Oliver syndrome (AOS) is characterized by the combination of congenital scalp defects (aplasia cutis congenita) and terminal transverse limb defects of variable severity. It is believed that Adams-Oliver syndrome without major organ abnormalities does not necessarily alter the normal lifespan. We present a case without detectable major organ abnormality contrary to life but with poor weight gain. A male infant with scalp and skin cutis aplasia, generalized cutis aplasia, dilated veins over scalp and trunk, hypoplastic toes and nails of feet, glaucoma, poor feeding and poor weight gain. This report shows a case of AOS without major multiple organ abnormalities but with poor feeding and abnormal weight gain that may be alter the normal lifespan.
机译:亚当斯-奥利夫综合征(AOS)的特征是先天性头皮缺损(先天性角膜缺乏症)和严重程度不同的末梢横肢缺损相结合。据信,没有重大器官异常的亚当斯-奥利弗综合症并不一定会改变正常寿命。我们提出的病例中没有发现与生命相反的主要器官异常,但体重增加较差。患有头皮和皮肤角质层发育不全,全身性角质层发育不全,头皮和躯干上的静脉扩张,脚趾和脚指甲发育不良,青光眼,喂养不良和体重增加不良的男性婴儿。该报告显示一例无严重多器官功能异常的AOS,但喂养不良且体重增加异常,可能会改变正常寿命。

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