Purpose: To describe the clinical features of eyes with elevated IOP and diagnosed with iridocorneal endothelial (ICE) syndrome. Subject: 30 eyes with elevated IOP and diagnosed with ICE syndrome of 28 patients were recruited. Method: Observation, retrospective study. Result: ICE syndrome usually diagnosed over the age of 40. 92.9 percent of patients is unilateral. This disease is asymptomatic at the early stage, it progresse slowly and can cause severe visual loss if left untreated. 86.7 percent of eyes has moderate elevated IOP (25-32mmHg), the number of endothelial cell is decresed. less than 1500 cell/mm2 in 86.6 percent of eyes. ICE syndrome has three main features: progressive iris atrophy. Cogan-Reese syndrome and Chandler's syndrome. Conclusion: ICE is usually diagnosed over the age of 40, unilateral with a variable injured level of cornea, iris and moderate elevated IOP.