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一名患有颅面短小畸形的儿童单侧冠状缝早闭病例。

A case of unilateral coronal synostosis in a child with craniofacial microsomia.

作者信息

Terry Michael J, Ascherman Jeffrey A

机构信息

Division of Plastic Surgery, Columbia College of Physicians and Surgeons, Columbia University Medical Center, 161 Fort Washington Avenue, New York, NY 10032, USA

出版信息

Cleft Palate Craniofac J. 2006 Nov;43(6):752-6. doi: 10.1597/05-159.

Abstract

Craniofacial microsomia is a congenital malformation complex associated with a wide array of craniofacial and extracraniofacial anomalies. Frontal plagiocephaly has been shown to occur in approximately 5% to 12% of patients with craniofacial microsomia. The etiology of craniofacial microsomia-associated frontal plagiocephaly is unclear; of the cases described in the literature, all but one had physical findings suggestive of deformational plagiocephaly. In the case with equivocal physical findings, radiographic studies showed no evidence of craniosynostosis. Unlike the above cases, we report a documented case of radiologically-confirmed unilateral coronal synostosis in a child with craniofacial microsomia.

摘要

颅面短小畸形是一种先天性畸形综合征,伴有一系列颅面和颅外异常。据显示,约5%至12%的颅面短小畸形患者会出现额部斜头畸形。颅面短小畸形相关的额部斜头畸形的病因尚不清楚;在文献中描述的病例中,除一例之外,所有病例的体格检查结果均提示为变形性斜头畸形。在体格检查结果不明确的该病例中,影像学研究未显示颅骨缝早闭的证据。与上述病例不同,我们报告了一例经放射学证实的单侧冠状缝早闭的病例,该患儿患有颅面短小畸形。

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