虹膜角膜内皮综合征(Iridocorneal Endothelial syndrome)是一种以虹膜基质进行性萎缩为主要表现的眼病,因角膜内皮细胞及后弹力膜异常增生掩盖小梁网和虹膜表面,以及周边虹膜前粘连而导致继发性青光眼。本病包括三种主要临床类型,即原发性虹膜萎缩症、Chandler氏综合征及虹膜痣综合征,但有不少病人为中间型,各型 Iridocorneal Endothelial Syndrome (Iridocorneal Endothelial syndrome) is an eye disease characterized by progressive atrophy of the iris stroma, which is caused by the corneal endothelial cells and the remodeling of the posterior amniotic membrane that mask the surface of the trabecular meshwork and the iris, and the peri-iris adhesions Secondary glaucoma. The disease includes three main clinical types, namely, primary iris atrophy, Chandler’s syndrome and iris nevus syndrome, but many patients are intermediate, all types