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首页> 外文期刊>The Journal of craniofacial surgery >Dolichocephaly without sagittal craniosynostosis
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Dolichocephaly without sagittal craniosynostosis

机译:无矢状颅突神经突

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摘要

Premature closure of the sagittal suture is thought to be fundamental to the etiopathology for the disease process called sagittal craniosynostosis. This process traditionally results in a well-known skull malformation termed dolichocephaly. Over recent decades, some authors have questioned the suture as the primary driving force for this pathology. This is a retrospective cases series of 4 patients from 2011 to 2012 who presented to the Yale Craniofacial Clinic for evaluation of dolichocephaly. The 4 children, 3 boys and 1 girl, had physical examinations and cranial indices concerning for sagittal craniosynostosis; however, subsequent computed tomographic imaging revealed sagittal suture patency. This series adds to a growing body of literature, which describes abnormal head shapes not attributable to overt suture pathology.
机译:矢状缝线的过早闭合被认为是被称为矢状颅突神经病的疾病过程的病因学基础。传统上,此过程会导致众所周知的头骨畸形,称为头足畸形。在最近的几十年中,一些作者质疑缝合线是这种病理学的主要驱动力。这是2011年至2012年的4例患者的回顾性病例系列,他们被提交给耶鲁颅面诊所以评估小头畸形。 4名儿童(3名男孩和1名女孩)接受了体检和颅骨指数检查,检查是否为矢状颅突。然而,随后的计算机体层摄影成像显示矢状缝通畅。该系列增加了越来越多的文献,这些文献描述了并非归因于明显缝合病理的异常头部形状。

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