File:PMC3532175 1471-2350-13-104-1.png

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Attribution 2.0 Generic (CC BY 2.0)

Summary

Author:Bendon CL, Fenwick AL, Hurst JA, Nürnberg G, Nürnberg P, Wall SA, Wilkie AO, Johnson D ,Oxford Craniofacial Unit, Oxford University Hospitals NHS Trust, John Radcliffe Hospital (Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC3532175_1471-2350-13-104-1&query=Chromosome%205q%20deletion%20syndrome&it=xg&req=4&npos=30 Description:F1: A-D: Patient 1.A: Antero-posterior (AP) view showing facial features including hypertelorism. B: Lateral view showing brachycephaly and micrognathia. C: X-ray (XR) right radius/ulna showing broad appearance of the radius at the junction between the proximal and middle thirds. D: XR left hand showing crowding of the carpal bones, broad metacarpals, proximal and middle phalanges, and flexion at the MCP and PIP joints. E-G: Patient 2.E: AP view showing facial features including hypertelorism. F: Lateral view showing brachycephaly. G: 3D CT scan showing absence of the sagittal suture. H-J: Patient 3.H: AP view showing facial features including hypertelorism. I: Lateral view showing class III malocclusion and brachycephaly. J: 3D CT scan showing absence of the sagittal suture.