Iridocorneal endothelial syndrome.

被引:0
|
作者
Halhal, M
D'Hermies, F [1 ]
Morel, X
Renard, G
机构
[1] Hop Dieu Paris, Serv Ophtalmol, F-75181 Paris 04, France
[2] Hop Specialites, Serv Ophtalmol B, Rabat, Morocco
来源
JOURNAL FRANCAIS D OPHTALMOLOGIE | 2001年 / 24卷 / 06期
关键词
ICE syndrome; Cogan-Reese syndrome; iris essentiel atrophy syndrome;
D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
The ICE syndrome includes 3 variants of the same disease, previously believed to be independent entities. All 3 share clinical and histopathological features such as endothelial abnormalities, iris damage, and progressive closure of the iridocorneal angle. Seven cases of ICE syndrome are reported, affecting 6 women and 1 man, with a mean age of 40 years. Corectopia was found in 5 eyes, a uveal ectropion in 2 cases, and other iris changes in 3 cases. The endothelial changes of the cornea were confirmed by a speculum microscopy in 5 cases. There were 5 cases of Chandler syndrome, 1 of Cogan-Reese syndrome, and 1 case of iris essentiel atrophy in our series. ocular hypertony was observed in 3 cases, 2 of which needed to be operated. in one patient, a corneal edema was observed.
引用
收藏
页码:628 / 634
页数:7
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