Kabuki syndrome: a review

被引:136
作者
Adam, MP [1 ]
Hudgins, L [1 ]
机构
[1] Stanford Univ, Div Med Genet, Stanford, CA 94305 USA
关键词
Kabuki make-up syndrome; Kabuki syndrome; Niikawa-Kuroki syndrome;
D O I
10.1111/j.1399-0004.2004.00348.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Kabuki syndrome (KS) (Kabuki make-up syndrome, Niikawa-Kuroki syndrome) is a multiple malformation/mental retardation syndrome that was described initially in Japan but is now known to occur in many other ethnic groups. It is characterized by distinctive facial features (eversion of the lower lateral eyelid, arched eyebrows with the lateral one-third dispersed or sparse, depressed nasal tip, and prominent ears), skeletal anomalies, dermatoglyphic abnormalities, short stature, and mental retardation. A number of other manifestations involving other organ systems can aid in the diagnosis and management of KS. This review will focus on the diagnostic criteria, the common and rare features of KS by organ system, and the possible etiology of this interesting condition.
引用
收藏
页码:209 / 219
页数:11
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