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婴儿非综合征性单侧冠状缝早闭的颅面畸形。

Craniofacial Dysmorphology in Infants With Non-Syndromic Unilateral Coronal Craniosynostosis.

机构信息

Division of Plastic and Reconstructive Surgery, Icahn School of Medicine at Mount Sinai.

Division of Paleontology, American Museum of Natural History, New York, NY.

出版信息

J Craniofac Surg. 2022 Sep 1;33(6):1903-1908. doi: 10.1097/SCS.0000000000008464. Epub 2022 Jan 10.

Abstract

BACKGROUND

Unilateral coronal craniosynostosis (UCS) is a congenital disorder resulting from the premature suture fusion, leading to complex primary and compensatory morphologic changes in the shape of not only the calvarium and but also into the skull base. This deformity typically requires surgery to correct the shape of the skull and prevent neurologic sequelae, including increased intracranial pressure, sensory deficits, and cognitive impairment.

METHODS

The present multicenter study sought to reverse-engineer the bone dysmorphogenesis seen in non-syndromic UCS using a geometric morphometric approach. Computed tomography scans for 26 non-syndromic UCS patients were converted to three-dimensional mesh models. Two hundred thirty-six unique anatomical landmarks and semi-landmarked curves were then plotted on each model, creating wireframe representations of the Patients' skulls.

RESULTS

Generalized Procrustes superimposition, Principal Component Analysis, and heatmaps identified significant superior displacement of the ipsilateral orbit ("harlequin" eye deformity), anterior displacement of the ear ipsilateral to the fused coronal suture, acute deviation of midline skull base structures ipsilateral to the fused coronal suture and flattening of the parietal bone and associated failure to expand superiorly.

CONCLUSIONS

The described technique illustrates the impact of premature coronal suture fusion on the development of the entire skull and proposes how bone dysmorphology contributes to the Patients' neurologic sequelae. By bridging novel basic science methodologies with clinical research, the present study quantitatively describes craniofacial development and bone dysmorphogenesis.

摘要

背景

单侧冠状缝早闭(UCS)是一种先天性疾病,由于缝线过早融合导致颅骨和颅底的形态发生复杂的原发性和代偿性变化。这种畸形通常需要手术矫正颅骨形状,以预防神经后遗症,包括颅内压升高、感觉缺失和认知障碍。

方法

本多中心研究旨在使用几何形态测量学方法对非综合征性 UCS 所见的骨发育不良进行逆向工程。对 26 例非综合征性 UCS 患者的计算机断层扫描进行转换,生成三维网格模型。然后在每个模型上绘制 236 个独特的解剖标志点和半标志曲线,创建患者颅骨的线框表示。

结果

广义 Procrustes 叠加、主成分分析和热图确定了同侧眼眶的明显向上移位(“小丑”眼畸形)、同侧冠状缝融合的耳的前移位、同侧中线颅底结构的锐角偏斜、融合冠状缝和顶骨变平以及未能向上扩张。

结论

描述的技术说明了过早的冠状缝融合对整个颅骨发育的影响,并提出了骨发育不良如何导致患者的神经后遗症。通过将新的基础科学方法与临床研究相结合,本研究定量描述了颅面发育和骨发育不良。

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