多余的
遗传学
少汗性外胚层发育不良
突变
生物
无义突变
Wnt信号通路
多指
基因
解剖
错义突变
作者
Worawan Kunotai,Panjit Ananpornruedee,Mark Lubinsky,Apitchaya Pruksametanan,Piranit Nik Kantaputra
摘要
A Thai mother and her two daughters were affected with tricho‐rhino‐phalangeal syndrome type I. The daughters had 15 and 18 supernumerary teeth, respectively. The mother had normal dentition. Mutation analysis of TRPS1 showed a novel heterozygous c.3809_3811delACTinsCATGTTGTG mutation in all. This mutation is predicted to cause amino acid changes in the Ikaros‐like zinc finger domain near the C‐terminal end of TRPS1 , which is important for repressive protein function. The results of our study and the comprehensive review of the literature show that pathways of forming supernumerary teeth appear to involve APC and RUNX2 , the genes responsible for familial adenomatous polyposis syndrome and cleidocranial dysplasia, respectively. The final pathway resulting in supernumerary teeth seems to involve Wnt, a morphogen active during many stages of development. © 2016 Wiley Periodicals, Inc.
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