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凯珀特综合征的另一病例及文献综述。

Additional case of Keipert syndrome and review of the literature.

作者信息

Cappon S M, Khalifa M M

机构信息

Department of Paediatrics, Queen's University and Kingston General Hospital, Kingston, Canada.

出版信息

Med Sci Monit. 2000 Jul-Aug;6(4):776-8.

Abstract

We report on a 7-year-old boy with unusual facial features, severe bilateral sensorineural hearing loss, and broad terminal phalanges. These findings are similar to those described by Keipert et al. in two brothers and by Balci and Dagli in two other male siblings. Our patient has, in addition, developmental delay and abnormal behaviour. To the best of our knowledge, this is only the third report of Keipert syndrome.

摘要

我们报告了一名7岁男孩,他具有不寻常的面部特征、严重的双侧感音神经性听力损失和宽阔的指端。这些发现与Keipert等人在两兄弟中以及Balci和Dagli在另外两名男性同胞中所描述的相似。此外,我们的患者有发育迟缓及行为异常。据我们所知,这是关于Keipert综合征的第三篇报道。

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