首页> 外文期刊>The Journal of craniofacial surgery >Normally shaped heads with no sutures, normally shaped heads with abnormal sutures, and abnormally shaped heads with normal sutures.
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Normally shaped heads with no sutures, normally shaped heads with abnormal sutures, and abnormally shaped heads with normal sutures.

机译:没有缝线的正常形状的头,具有异常缝线的正常形状的头和具有正常缝线的异常形状的头。

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摘要

We present a series of children whose head shapes and suture status do not make sense. There were 3 patients with complete absence of sutures and normal head shapes. One patient was evaluated for microcephaly at 6 years of age. In the second, the absence of sutures was discovered on workup for headaches at 8 years of age. The third underwent x-ray imaging for parasagittal bony nodules at 1 month of age. The head circumferences fell at the 4th, 25th, and 50th percentiles, respectively. The 2 older children were in normal classes, and the youngest was meeting milestones appropriately. We encountered 3 patients with fusion of the sagittal suture and normal head shapes. One had a flattened occiput, the second patient was thought to be brachycephalic, and the third was macrocephalic. Head circumferences were at the fourth, 50th, and 75th percentiles. The patient with head circumference at the fourth percentile had fetal alcohol syndrome and speech delay. The other 2 were developing normally with follow-up of 14 months. Finally, 3 patients underwent surgery for characteristic craniosynostotic head shapes and were found to have patent sutures at surgery. One patient had classic unilateral coronal synostosis and a patent suture on the side of the defect. The second patient had Crouzon syndrome with characteristic head shape, but open coronal sutures. The third patient had the appearance of bicoronal synostosis, with a patent suture on one side. They have had good results from their craniofacial reconstructions at 24, 12, and 6 months' follow-up. CONCLUSIONS: We have no explanation for these interesting findings.
机译:我们介绍了一系列头部形状和缝合状态不合理的孩子。有3例完全没有缝合且头部形状正常的患者。对一名患者在6岁时进行了小头畸形评估。第二,在检查中发现在8岁时因头痛而没有缝合线。第三例在1个月大时接受了X线成像,用于矢状旁矢状结节。头围分别下降了第4、25和50个百分点。 2个年龄较大的孩子在正常上课,而最小的孩子正在适当地达到里程碑。我们遇到了3例矢状缝线融合和正常头部形状的患者。一个人的枕骨扁平,第二个病人被认为是头颅畸形,第三个病人是大头颅。头围分别位于第四,第50和第75个百分点。头围在第四个百分点的患者患有胎儿酒精综合症和语言障碍。其他2例进展正常,随访14个月。最终,有3例因颅骨突触的头部形状特征接受了手术,并在手术中发现了缝合线。一名患者患有典型的单侧冠状动脉滑膜炎,并在缺损一侧缝合了一条缝线。第二例患者患有克罗赞综合征,头部特征明显,但冠状缝线开放。第三例患者出现双冠状突触,一侧有缝线。他们在术后24、12和6个月的颅面重建术中均取得了良好的效果。结论:我们没有解释这些有趣的发现。

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