Current treatment of craniosynostosis and future therapeutic directions.

D. Wan, Matthew D. Kwan, H. Lorenz, M. Longaker
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引用次数: 13

Abstract

Normal craniofacial development is contingent upon coordinated growth between the brain and overlying calvaria. Craniosynostosis, the premature fusion of one or more cranial sutures, perturbs this natural framework, resulting in dramatic dysmorphology of the skull and face along with a multitude of associated functional abnormalities. Traditional approaches to the treatment of craniosynostosis have employed complex surgical remodeling of the skull vault and facial deformities all aimed at increasing the amount of intracranial volume and restoring a more normal craniofacial appearance. Significant morbidity and mortality, however, have plagued these procedures, driving dramatic evolution in our approach towards the treatment of pathologically fused sutures. Recent clinical and genetic studies have identified multiple forms of human craniosynostosis, each associated with mutations within various cytokine signaling pathways. Knowledge garnered from these investigations bear promise for the future development of alternative strategies to enhance or perhaps even replace contemporary approaches for the treatment of craniosynostosis.
颅缝闭锁的治疗现状及未来治疗方向。
正常的颅面发育取决于大脑和上覆颅骨之间的协调生长。颅缝闭合症,即一条或多条颅缝的过早融合,扰乱了这种自然框架,导致颅骨和面部的严重畸形以及许多相关的功能异常。颅缝闭锁的传统治疗方法采用复杂的颅骨拱顶手术重塑和面部畸形,目的是增加颅内容积,恢复更正常的颅面外观。然而,严重的发病率和死亡率一直困扰着这些手术,促使我们在治疗病理性融合缝合线的方法上发生了巨大的变化。最近的临床和遗传学研究已经确定了人类颅缝闭锁的多种形式,每种形式都与各种细胞因子信号通路中的突变有关。从这些调查中获得的知识为未来发展替代策略提供了希望,以加强甚至取代颅缝闭锁的当代治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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