Iridocorneal endothelial syndrome
(Redirected from Cogan-Reese syndrome)
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Jyostna Chouturi, M.B.B.S [2]
Overview
Iridocorneal endothelial or ICE syndrome is a spectrum of conditions of the eye,[1] where the inner layer of the cornea appears abnormal.[2] It includes Cogan-Reese syndrome, Chandler's syndrome, and progressive iris atrophy.
Historical Prospective
"Cogan-Reese syndrome" is named for David Glendenning Cogan and Algernon Reese.[3][4]
References
- ↑ Lefebvre V, Sowka JW, Frauens BJ (August 2009). "The clinical spectrum between posterior polymorphous dystrophy and iridocorneal endothelial syndromes". Optometry. 80 (8): 431–6. doi:10.1016/j.optm.2009.02.009. PMID 19635434.
- ↑ Mastering the Techniques of Glaucoma Diagnosis and Management. Jaypee Brothers Medical Publishers (P) Ltd. 2006. ISBN 81-8061-758-0.
- ↑ Template:WhoNamedIt
- ↑ Cogan DG, Reese AB (1969). "A syndrome of iris nodules, ectopic Descemet's membrane, and unilateral glaucoma". Doc Ophthalmol. 26: 424–33. doi:10.1007/bf03186675. PMID 5359536.
External links
- Facts About the Cornea and Corneal Disease The National Eye Institute (NEI).