Ganesh Anuradha, Al-Kindi Adila, Jain Rajeev, Raeburn Sandy
Department of Ophthalmology, Sultan Qaboos University Hospital, Muscat, Oman.
J AAPOS. 2005 Dec;9(6):604-6. doi: 10.1016/j.jaapos.2005.05.001.
The syndrome of iris coloboma, ptosis, hypertelorism, and mental retardation (Online Mendelian Inheritance in Man -- OMIM # 243310), also known as the Baraitser-Winter syndrome, originally was described in a brother and sister and in an unrelated girl in 1988. Six additional individuals with a similar phenotype have been reported in the world literature. Microphthalmos, microcornea, and brain malformations were added to the phenotypic spectrum of this syndrome in 1995. We report a child who presented with the aforementioned findings. Eye examination revealed bilateral microphthalmos and typical iris, optic nerve, and choroidal colobomas. Magnetic resonance imaging of the brain demonstrated pachygyria and cortical atrophy.
虹膜缺损、上睑下垂、眼距过宽和智力发育迟缓综合征(《人类孟德尔遗传在线》——OMIM # 243310),也称为巴拉伊泽-温特综合征,最初于1988年在一对兄妹和一名无血缘关系的女孩中被描述。世界文献中还报道了另外6名具有相似表型的个体。1995年,小眼症、小角膜和脑畸形被纳入该综合征的表型谱。我们报告一名出现上述表现的患儿。眼部检查发现双侧小眼症以及典型的虹膜、视神经和脉络膜缺损。脑部磁共振成像显示巨脑回和皮质萎缩。