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常染色体显性遗传性舌系带过短和牙齿数目异常。

Autosomal-dominant ankyloglossia and tooth number anomalies.

机构信息

Oral Care Center for Inherited Diseases, University Hospital of Brasilia, Department of Dentistry, University of Brasilia, Brazil.

出版信息

J Dent Res. 2010 Feb;89(2):128-32. doi: 10.1177/0022034509356401. Epub 2009 Dec 30.

Abstract

Ankyloglossia is a congenital oral anomaly characterized by the presence of a hypertrophic lingual frenulum. It frequently accompanies X-linked cleft palate and is sometimes seen alone due to mutations in the gene encoding the transcription factor TBX22, while knockout of Lgr5 in the mouse results in ankyloglossia. The aim of the present study was to characterize the phenotype and to verify sequence variations in the LGR5 gene in a Brazilian family with ankyloglossia associated with tooth number anomalies. Twelve individuals of three generations were submitted to physical, oral, and radiographic examinations and molecular analysis. Eight had ankyloglossia with various degrees of severity. Six also had hypodontia in the lower incisor region; one had a supernumerary tooth in this region, and another had a supernumerary tooth in the lower premolar region. The characterization of this family determined an autosomal-dominant inheritance and excluded the LGR5 gene mutations as being involved in the pathogenesis of this condition.

摘要

舌系带过短是一种先天性口腔异常,其特征是存在肥大的舌系带。它常伴有 X 连锁腭裂,有时也单独出现,这是由于编码转录因子 TBX22 的基因突变所致,而在小鼠中敲除 Lgr5 则会导致舌系带过短。本研究的目的是描述一个巴西舌系带过短伴牙齿数量异常家族的表型,并验证 LGR5 基因的序列变异。三代共 12 人接受了体格、口腔和影像学检查及分子分析。8 人有不同程度的舌系带过短。6 人下颌切牙区有先天性缺牙,1 人下颌切牙区有多生牙,另 1 人下颌前磨牙区有多生牙。对这个家系的特征分析确定为常染色体显性遗传,排除了 LGR5 基因突变与该疾病发病机制的关系。

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