锁骨颅骨发育不全患者的多颗埋伏牙和多生牙。

Multiple unerupted and supernumerary teeth in a patient with cleidocranial dysplasia.

作者信息

Omami Galal

机构信息

Department of Oral Health Practice, Division of Oral Medicine, Diagnosis and Radiology, University of Kentucky College of Dentistry, 800 Rose Street, Room MN-320, Lexington, KY 40536-0297, USA.

出版信息

Radiol Case Rep. 2017 Dec 7;13(1):118-120. doi: 10.1016/j.radcr.2017.11.009. eCollection 2018 Feb.

DOI:10.1016/j.radcr.2017.11.009

PMID:29487646

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5826465/

Abstract

Cleidocranial dysplasia is an extremely rare familial disorder characterized by partial or complete absence of clavicles, characteristic craniofacial deformities, and the presence of numerous supernumerary and unerupted teeth. Here, the author reviews the striking radiographic findings of cleidocranial dysplasia in a 16-year-old adolescent boy who presented with delayed teeth eruption.

摘要

锁骨颅骨发育不全是一种极其罕见的家族性疾病，其特征为部分或完全没有锁骨、典型的颅面畸形以及存在大量多生牙和未萌出的牙齿。在此，作者回顾了一名16岁青春期男孩锁骨颅骨发育不全的显著影像学表现，该男孩表现为牙齿萌出延迟。