File:PMC4231219 dmcn0056-0627-f1.png

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PMC4231219_dmcn0056-0627-f1.png ‎(512 × 221 pixels, file size: 256 KB, MIME type: image/png)

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Attribution 3.0 Unported (CC BY 3.0)

Summary

Author:Kurian MA, Jungbluth H,Developmental Neurosciences, UCL-Institute of Child Health, London, UK; Department of Neurology, Great Ormond Street Hospital for Children (Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC4231219_dmcn0056-0627-f1&query=Allan-Herndon-Dudley%20syndrome&it=xg&req=4&npos=1 Description:fig01: A 4-year-old patient with genetically confirmed Allan-Herndon-Dudley syndrome, with photographs illustrating (a) face/trunk/limbs (b) facial features and (c) lateral facial view. Note the typical but subtle dysmorphic features, including myopathic facial appearance with inverted V-shaped mouth, low anterior hairline, narrow forehead, receding chin, and large, low-set ears. From Gika et al.,17 with permission.

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Date/TimeThumbnailDimensionsUserComment
current21:55, 14 November 2021Thumbnail for version as of 21:55, 14 November 2021512 × 221 (256 KB)Ozzie10aaaaAuthor:Kurian MA, Jungbluth H,Developmental Neurosciences, UCL-Institute of Child Health, London, UK; Department of Neurology, Great Ormond Street Hospital for Children (Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC4231219_dmcn0056-0627-f1&query=Allan-Herndon-Dudley%20syndrome&it=xg&req=4&npos=1 Description:fig01: A 4-year-old patient with genetically confirmed Allan-Herndon-Dudley syndrome, with photographs illustrating (a) face/trunk/limbs (b) f...

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