File:Apert syndrome or type I acrocephalosyndactyly (Radiopaedia 9731-10342 A 1).jpg

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Apert_syndrome_or_type_I_acrocephalosyndactyly_(Radiopaedia_9731-10342_A_1).jpg ‎(400 × 479 pixels, file size: 113 KB, MIME type: image/jpeg)

Summary:

Description
  • Radiopaedia case ID: 9731
  • Image ID: 454496
  • Study findings: Bracycephaly and midface hypoplasia with premature fusion of the coronal suture and abnormal widening of the sagittal suture.
  • Modality: CT
  • System: Paediatrics
  • Findings: Bilateral acrocephalosyndactyly
Date Published: 16th May 2010
Source https://radiopaedia.org/cases/apert-syndrome-or-type-i-acrocephalosyndactyly
Author Hani Makky Al Salam
Permission
(Permission-reusing-text)		 http://creativecommons.org/licenses/by-nc-sa/3.0/

Licensing:

Attribution-NonCommercial-ShareAlike 3.0 Unported (CC BY-NC-SA 3.0)

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current07:06, 19 May 2021Thumbnail for version as of 07:06, 19 May 2021400 × 479 (113 KB)Fæ (talk | contribs)Radiopaedia project rID:9731 (batch #2587-1 A1)

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