综合征型颅缝闭闭的临床特点。

D. Rice
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引用次数: 33

摘要

正常缝线发育和功能的破坏可导致缝线过早融合,颅缝闭合。这篇综述的重点是颅缝闭锁的综合征形式。以颅缝闭锁为特征的综合征超过100种,本文描述了包括Apert和Crouzon综合征在内的最常见病症,以及具有特别有趣的分子病因的其他病症,如Saethre- Chotzen和颅额鼻综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical features of syndromic craniosynostosis.
Disruption of normal suture development and function can result in premature suture fusion, craniosynostosis. This review focuses on syndromic forms of craniosynostosis. More than 100 syndromes in which craniosynostosis is a feature have been documented and here the most common conditions including Apert and Crouzon syndromes are described as well as other conditions with a particularly interesting molecular etiology, such as Saethre- Chotzen and craniofrontonasal syndrome.
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