OPITZ (BBB/G) SYNDROME - ORAL MANIFESTATIONS

被引:26
作者
BROOKS, JK [1 ]
LEONARD, CO [1 ]
COCCARO, PJ [1 ]
机构
[1] UNIV UTAH,SCH MED,DEPT PEDIAT,SALT LAKE CITY,UT 84112
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 43卷 / 03期
关键词
G-SYNDROME; HYPERTELORISM; HYPOSPADIAS; LARYNGOTRACHEOESOPHAGEAL DEFECTS; ORAL MANIFESTATIONS;
D O I
10.1002/ajmg.1320430318
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We studied a new case of the G (Opitz BBB/G) syndrome in a 12-year-old boy. Several relatives had partial manifestations of the disorder. A comprehensive dental evaluation of the propositus was conducted; included is, to our knowledge, the first published cephalometric analysis of a G syndrome patient. We reviewed 139 cases of the G syndrome; 48 of them had at least one oral abnormality. These included clefting, micrognathia, ankyloglossia, and high-arched palate. Male G syndrome patients are more likely to have oral anomalies than affected females.
引用
收藏
页码:595 / 601
页数:7
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