File:Apert syndrome - prenatal findings (Radiopaedia 64670).jpg

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Summary:

Description
  • Radiopaedia case ID: 64670
  • Image ID: 44397438
  • Modality: Ultrasound
  • System: Obstetrics
  • Findings: Images 1 and 2 revealed mild ventricular dilation, normal cavum, and normal posterior fossa.Images 3-7 revealed an abnormal face with frontal bossing with a tendancy to turribrachycephaly and hypertelorism. Images 8 and 9 revealed complex syndactyly with “mitten” and “rosebud” external appearance.Our prenatal diagnosis was Apert Syndrome, a kind of syndromic craniosynostosis.
Date Published: 10th Dec 2018
Source https://radiopaedia.org/cases/apert-syndrome-prenatal-findings-2
Author Fabien Ho
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 2021958 × 654 (140 KB)Fæ (talk | contribs)Radiopaedia project rID:64670 (batch #2588)

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