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非综合征性多生牙的家族性发病。一种罕见病症。

Familial occurrence of nonsyndromal multiple supernumerary teeth. A rare condition.

作者信息

Orhan Ayşe Işil, Ozer Levent, Orhan Kaan

机构信息

Department of Pediatric Dentistry, University of Ankara, Ankara, Turkey.

出版信息

Angle Orthod. 2006 Sep;76(5):891-7. doi: 10.1043/0003-3219(2006)076[0891:FOONMS]2.0.CO;2.

Abstract

The occurrence of multiple supernumerary teeth is a rare phenomenon and is often found in association with syndromes such as cleidocranial dysplasia, Gardners syndrome, or cleft lip and palate. Only a few examples of nonsyndromal multiple supernumerary teeth have been reported in the literature. There is a predilection for the mandible and in the premolar area followed by the molar and anterior regions. This article reports the presence of nonsyndromal multiple supernumerary teeth involving both jaws in children and in their mothers. The clinical and radiographic appearance of the anomalies and treatment modalities are discussed.

摘要

多生牙的出现是一种罕见现象,常与锁骨颅骨发育不全、加德纳综合征或唇腭裂等综合征相关。文献中仅报道了少数非综合征性多生牙的病例。多生牙在下颌及前磨牙区最为常见,其次是磨牙区和前牙区。本文报道了儿童及其母亲非综合征性多生牙累及上下颌的病例。文中讨论了这些异常的临床和影像学表现以及治疗方式。

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