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与杜普伊特伦挛缩症相关的家族性牙发育不全。

Familial hypodontia associated with Dupuytren's disease.

作者信息

Ranta H, Knif J, Ranta K

机构信息

Department of Cariology, University of Helsinki, Finland.

出版信息

Scand J Dent Res. 1990 Dec;98(6):457-60. doi: 10.1111/j.1600-0722.1990.tb00999.x.

Abstract

A three-generation Finnish family exhibited hypodontia associated with Dupuytren's disease (contracture). Of the known 32 members of the family, contracture has been diagnosed thus far in 5 individuals, 4 of these also with hypodontia. No other connective tissue involvement was found. For comparison, three other families were studied, also showing incomplete penetrance of hypodontia. Bearing in mind the genetic isolation of the Finnish population, this finding may be coincidental. The possibility of partially common genetic background cannot, however, be excluded.

摘要

一个三代芬兰家庭出现了与杜普伊特伦挛缩病(掌挛缩病)相关的牙发育不全。在该家族已知的32名成员中,迄今为止已有5人被诊断患有挛缩病,其中4人还患有牙发育不全。未发现其他结缔组织受累情况。作为对照,还研究了其他三个家庭,也显示出牙发育不全的不完全外显率。考虑到芬兰人群的遗传隔离情况,这一发现可能是巧合。然而,部分共同遗传背景的可能性也不能排除。

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