File:PMC4640438 1657-9534-cm-46-03-00150-gf04.png

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PMC4640438_1657-9534-cm-46-03-00150-gf04.png (328 × 376 pixels, file size: 207 KB, MIME type: image/png)

Captions

Captions

Apert Syndrome

Summary

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Description
English: f04: A. Male patient (II, 2) diagnosed with Apert Syndrome. Craniofacial features includes midface hypoplasia, low-set ears, depressed nose bridge, turricephaly, and osseous syndactyly in hands and feet. B. Skull computer tomography (CT) with three-dimensional (3D) model reconstruction of patient II, 2, Family 1. Several sutures synostosis (blue box) and midface hypoplasia shown in lateral (1) and frontal (2) images.
Date
Source https://openi.nlm.nih.gov/detailedresult?img=PMC4640438_1657-9534-cm-46-03-00150-gf04&query=Apert%20syndrome&it=xg&req=4&npos=2
Author Torres L, Hernández G, Barrera A, Ospina S, Prada R

Licensing

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w:en:Creative Commons
attribution
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current20:44, 23 July 2023Thumbnail for version as of 20:44, 23 July 2023328 × 376 (207 KB)Ozzie10aaaa (talk | contribs)Uploaded a work by Torres L, Hernández G, Barrera A, Ospina S, Prada R from https://openi.nlm.nih.gov/detailedresult?img=PMC4640438_1657-9534-cm-46-03-00150-gf04&query=Apert%20syndrome&it=xg&req=4&npos=2 with UploadWizard

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