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作 者:Vanita Pathak Ray Divya P Rao Isha Gulati
机构地区:[1]Centre For Sight,Banjara Hills,Hyderabad 500034,India [2]L V Prasad Eye Institute,Banjara Hills,Hyderabad 500034,India
出 处:《International Journal of Ophthalmology(English edition)》2019年第11期1809-1811,共3页国际眼科杂志(英文版)
摘 要:Dear Editor,I ridocorneal endothelial syndrome(ICE)is a rare,usually unilateral,acquired condition,hypothesized to be secondary to a viral etiology[1].It affects females more often than males and comprises of three distinct clinical types related to endothelial proliferation and its structural abnormalities.Proliferation of endothelium over the iridocorneal angle leads to progressive secondary angle closure and that over the iris leads to typical changes of polycoria and atrophy.Three clinical entities included in the syndrome are Chandlers(predominant corneal involvement),progressive iris atrophy(predominant iris involvement with polycoria and‘holes’)and Cogan Reese(iris nodules with loss of stromal features).No matter what the clinical type,it is a progressive condition and controlling intraocular pressure(IOP)and maintaining corneal clarity in the long term is usually a challenge.
关 键 词:CORNEAL INVOLVEMENT predominant
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