Aicardi syndrome: Chorioretinal lacunae without corpus callosum agenesis

被引：9

作者：

Iturralde, Diana ^{[1
]}

Meyerle, Catherine B. ^{[1
]}

Yannuzzi, Lawrence A. ^{[1
]}

机构：

[1] Manhattan Eye Ear & Throat Hosp, LuEsther T Mertz Retinal Res Ctr, Vitreous Retina Macula Consultants New York, New York, NY 10021 USA

来源：

RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES | 2006年 / 26卷 / 08期

关键词：

chorioretinal lacunae; Aicardi syndrome; corpus callosum agenesis;

D O I：

10.1097/01.iae.0000224937.78389.15

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

Aicardi syndrome (AS) was originally described in 1965 as a congenital abnormality with a classic triad of total or partial agenesis of the corpus callosum, infantile spasms, and chorioretinal lacunae.(1) In 2005, Aicardi(2) reported that the funduscopic findings are considered pathognomonic. We report a case of AS without corpus callosurn agenesis that was diagnosed on the basis of chorioretinal lacunae.

引用

页码：977 / 978

页数：2

共 5 条

[1] Aicardi syndrome [J].