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Additional case of Keipert syndrome and review of the literature

机译:Keipert综合征的其他病例并进行文献复习

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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.
机译:我们报告了一个7岁的男孩,其面部特征异常,严重的双侧感觉神经性听力减退和广泛的指骨狭窄。这些发现与Keipert等人的描述相似。在两个兄弟中,以及Balci和Dagli在另外两个男性同胞中。此外,我们的患者有发育迟缓和异常行为。据我们所知,这只是Keipert综合征的第三次报告。

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