Craniofacial and dental characteristics of Kabuki syndrome

被引:0
作者
Matsune, K
Shimizu, T
Tohma, T
Asada, Y
Ohashi, H
Maeda, T
机构
[1] Nihon Univ, Sch Dent, Dept Pediat Dent, Matsudo, Chiba 2718587, Japan
[2] Saitama Childrens Med Ctr, Div Med Genet, Iwatsuki, Saitama, Japan
[3] Univ Ryukyus, Sch Med, Dept Pediat, Uehara, Japan
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 98卷 / 02期
关键词
Kabuki syndrome; oral abnormality; hypodontia; cephalometric analysis;
D O I
10.1002/1096-8628(20010115)98:2<185::AID-AJMG1029>3.0.CO;2-M
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe oral manifestations in six patients (three females and three males aged 6 to 24 years) with Kabuki syndrome (KS), based on their physical, orthopantomographic, and cephalometric findings. All six patients had a high-arched palate, malocclusion, most commonly unilateral posterior cross-bite (5/6), severe maxillary recession and mid-facial hypoplasia, Other frequently observed oral manifestations included small dental arch and hypodontia. Three patients lacked permanent teeth, mostly the central/lateral incisors. Both tooth size (in primary and permanent teeth) and dental arch (in length and width) tended to be small. We would like to stress that oral care and management is a must for the well-being of KS patients. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:185 / 190
页数:6
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