Coloboma and other ophthalmologic anomalies in Kabuki syndrome: Distinction from charge association

被引:47
作者
Ming, JE
Russell, KL
Bason, L
McDonald-McGinn, DM
Zackai, EH
机构
[1] Childrens Hosp Philadelphia, Dept Pediat, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
关键词
Kabuki syndrome; multiple congenital abnormalities; eye abnormalities;
D O I
10.1002/ajmg.a.20277
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Kabuki (Niikawa-Kuroki) syndrome is associated with growth retardation, developmental delay, congenital heart disease, cleft palate, and characteristic facial features. Although the external appearance of the eyes has been well-described, the type and frequency of structural and functional eye anomalies has not been emphasized. We report three children with Kabuki syndrome who also had a retinal coloboma. A diagnosis of CHARGE association was initially suggested in two of the patients before the typical facial features of Kabuki syndrome emerged. A detailed review of reported cases of Kabuki syndrome shows that a variety of eye anomalies are associated with Kabuki syndrome. The incidence of coloboma is greatly increased in Kabuki syndrome. Thus, ophthalmologic abnormalities are frequently associated with Kabuki syndrome, and an ophthalmologic evaluation should be performed for each patient. Phenotypic overlap, including congenital heart, ear, and renal defects, can lead to the diagnosis of CHARGE association, especially since the typical facial features of Kabuki syndrome may not be apparent in early infancy. Thus, Kabuki syndrome should be considered in patients with coloboma if other features consistent with this condition are present, and follow-up evaluations are indicated for establishing the proper diagnosis. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:249 / 252
页数:4
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