File:PMC3791821 eplasty13e52 fig1.png

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PMC3791821_eplasty13e52_fig1.png ‎(512 × 264 pixels, file size: 286 KB, MIME type: image/png)

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Attribution 2.0 Generic (CC BY 2.0)

Summary

Author:Chu KF, Sullivan SR, Taylor HO,Warren Alpert Medical School of Brown University(Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC3791821_eplasty13e52_fig1&query=Saethre-Chotzen%20syndrome&it=xg&req=4&npos=2 Description:F1: Three-month-old female patient with Saethre-Chotzen syndrome and bicoronal synostosis resulting in significant turribrachycephaly (a). The sagittal, lambdoid, and squamosal sutures were patent with a large fontanelle, characteristic of Saethre-Chotzen syndrome. Initial computed tomographic volume rendering shows bicoronal craniosynostosis (b).

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Date/TimeThumbnailDimensionsUserComment
current22:42, 13 November 2021Thumbnail for version as of 22:42, 13 November 2021512 × 264 (286 KB)Ozzie10aaaaAuthor:Chu KF, Sullivan SR, Taylor HO,Warren Alpert Medical School of Brown University(Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC3791821_eplasty13e52_fig1&query=Saethre-Chotzen%20syndrome&it=xg&req=4&npos=2 Description:F1: Three-month-old female patient with Saethre-Chotzen syndrome and bicoronal synostosis resulting in significant turribrachycephaly (a). The sagittal, lambdoid, and squamosal sutures were patent with a large fontanelle, charact...

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