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[A case of atypical iris corneal endothelial syndrome].

作者信息

Cheng Y Y, Cheng S M, Xu H J, Yin J, Chen H

机构信息

Hebei Eye Hospital, Hebei Key Laboratory of Ophthalmology, Hebei Clinical Medical Research Center of Eye Diseases, Xingtai 054001, China.

出版信息

Zhonghua Yan Ke Za Zhi. 2022 Feb 11;58(2):146-148. doi: 10.3760/cma.j.cn112142-20211216-00588.

Abstract

Iridocorneal endothelial syndrome is a rare ophthalmic disease, most of which are unilateral and common in women. The rate of misdiagnosis and missed diagnosis is relatively high due to its various clinical manifestations. In this case, the patient presented uncontrollable high intraocular pressure, corneal edema leading to difficult observation of corneal endothelium morphology, and accompanied by a small amount of iris neovascularization. No clearly diagnosis was made before glaucoma surgery. Further examination was performed after corneal clearance, and the final diagnosis was iris corneal endothelial syndrome (Chandler syndrome).

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