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Bilateral iridocorneal endothelial syndrome-Chandler’s syndrome:a case report and literature review

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摘要 Dear Editor,I ridocorneal endothelial syndrome(ICE)is a rare ocular disease first proposed by Eagle et al[1]in 1979.It is mainly characterized by corneal endothelial abnormalities,accompanied by iris atrophy,iris pigmented nodules and peripheral anterior synechiae.ICE syndrome is typically unilateral,and classified into three clinical variants based on the changes of the cornea and iris,including progressive iris atrophy,Chandler’s syndrome,and Cogan-Reese syndrome.
机构地区 Shenzhen Eye Hospital
出处 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2024年第4期773-776,共4页 国际眼科杂志(英文版)
基金 Supported by the National Natural Science Foundation of China(No.82271087) Science and Technology Innovation Committee of Shenzhen(No.JCYJ20190807153005579) Shenzhen Science and Technology Program(KCXFZ20230731093359004).
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