Kabuki syndrome: description of dental findings in 8 patients

被引:29
|
作者
Mhanni, AA
Cross, HG
Chudley, AE
机构
[1] Childrens Hosp, Sect Genet & Metab, Winnipeg, MB R3A 1S1, Canada
[2] Univ Manitoba, Dept Human Genet, Winnipeg, MB R3T 2N2, Canada
[3] Univ Manitoba, Dept Pediat & Child Hlth, Winnipeg, MB R3T 2N2, Canada
关键词
dental abnormalities; Kabuki syndrome; multiple congenital anomalies;
D O I
10.1034/j.1399-0004.1999.560211.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The cardinal features of Kabuki (Niikawa-Kuroki) syndrome (KS) include characteristic facial dysmorphic features, mild to moderate mental deficiency, skeletal abnormalities, dermatoglyphic abnormalities, and postnatal growth retardation. We identified 8 patients with KS in a genetics clinic over the past 5 years. All were Caucasians except for 2 who were of mixed Aboriginal and Caucasian descent. All had the facial gestalt, the dermatoglyphic abnormalities characteristic of the syndrome, and developmental delay. Dental abnormalities of permanent teeth were seen in all 8 cases; 6 had missing lower incisors. Five patients had uniquely abnormal upper incisor teeth shape; the upper incisors had a 'flat head' screwdriver-shaped appearance. Other dental abnormalities included missing lower lateral incisors, missing second premolars, and ectopic upper 6-year molars. We believe the presence of the unique dental findings will prove useful in the diagnostic assessment of individuals with KS.
引用
收藏
页码:154 / 157
页数:4
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