Carney S H, Brodsky M C, Good W V, Glasier C M, Greibel M L, Cunniff C
Department of Ophthalmology, University of Arkansas for Medical Sciences, Little Rock.
Surv Ophthalmol. 1993 May-Jun;37(6):419-24. doi: 10.1016/0039-6257(93)90139-x.
An eight-month-old girl with infantile spasms and apparent blindness had electroencephalographic findings compatible with Aicardi syndrome. In addition to optic nerve hypoplasia, there were multiple congenital retinal malformations in the right eye, including chorioretinal lacunae, anomalous retinal vessels, posterior scleral ectasia, and a peripheral fibrous ridge. Magnetic resonance imaging demonstrated agenesis of the corpus callosum, absence of the septum pellucidum, optic nerve and chiasmal hypoplasia, pachygyria, cortical heterotopias, colpocephaly, and hypoplasia of the cerebellar vermis. This patient illustrates the broad spectrum of cerebroretinal malformations now known to characterize Aicardi syndrome.
一名患有婴儿痉挛症且明显失明的八个月大女孩,其脑电图检查结果符合艾卡迪综合征。除视神经发育不全外,右眼还存在多种先天性视网膜畸形,包括脉络膜视网膜缺损、视网膜血管异常、后巩膜膨出以及周边纤维嵴。磁共振成像显示胼胝体发育不全、透明隔缺如、视神经和视交叉发育不全、巨脑回、皮质异位、脑室扩张以及小脑蚓部发育不全。该患者体现了目前已知的构成艾卡迪综合征特征的广泛脑视网膜畸形。