Results 141 to 150 of about 1,456,153 (176)

The Contralateral Eye in the Iridocorneal Endothelial (ICE) Syndrome

Ophthalmology, 1983
Examination of six cases of iridocorneal endothelial (ICE) syndrome revealed that all the patients had subclinical abnormalities in the fellow eye. Of the six, four patients had iris transillumination, four patients had significantly decreased outflow facility but without elevation of intraocular pressure, and all patients had corneal endothelial ...
C, Kupfer, M I, Kaiser-Kupfer, M, Datiles, L, McCain   +3 more
openaire   +2 more sources

Prognosis for Penetrating Keratoplasty in Iridocorneal Endothelial Syndrome

Journal of Refractive Surgery, 1993
ABSTRACT BACKGROUND: Iridocorneal endothelial syndrome is characterized by the proliferation and spreading of an abnormal corneal endothelial membrane across the iridocorneal angle and iris surface, resulting in iridocorneal adhesions, glaucoma, pupillary distortion, varying degrees of iris atrophy, and occasionally corneal decomposition with
P C, Chang, H K, Soong, M F, Couto, R F, Meyer, A, Sugar   +4 more
openaire   +2 more sources

Iridocorneal Endothelial Syndrome and Glaucoma

2010
Iridocorneal endothelial (ICE) syndrome represents a spectrum of disease, encompassing three clinical variations: Chandler’s syndrome, progressive iris atrophy, and Cogan-Reese syndrome. This acquired, unilateral disorder typically manifests in young to middle adulthood and predominantly affects women, although bilateral involvement and occurrence in a
Sarwat Salim, Peter A. Netland
openaire   +1 more source

A Comparison of the Clinical Variations of the Iridocorneal Endothelial Syndrome

Archives of Ophthalmology, 1989
Iridocorneal endothelial syndrome is generally considered to have three major variations: Chandler's syndrome, progressive (essential) iris atrophy, and the Cogan-Reese syndrome. To better understand the clinical significance of this classification, we studied the medical records of 37 consecutive patients from our practice, comparing the presentation ...
M C, Wilson, M B, Shields
openaire   +2 more sources

Features of the Iridocorneal Endothelial Syndrome on Confocal Microscopy

Cornea, 2005
To present a subtle case of iridocorneal endothelial (ICE) syndrome and discuss the utility of in vivo confocal microscopy in the evaluation of this disorder. Previous reports of the confocal microscopic features of ICE syndrome are reviewed.A 32-year-old man presented with decreased vision and halos.
Daniel C, Garibaldi, Oliver D, Schein, Albert, Jun   +2 more
openaire   +2 more sources

Macular Edema and Iridocorneal Endothelial Syndrome

Cornea, 2005
To report a case of cystoid macular edema (CME) in iridocorneal endothelial syndrome.Case report.The authors describe the clinical history and ocular examination of a 38-year-old woman with iridocorneal endothelial syndrome and CME. This association has never been reported before.
Hülya, Kocaoğlan, Nurten, Unlü, Ayfer, Kanpolat, Ilgaz S, Yalvaç, Mehmet A, Acar, Sunay, Duman   +5 more
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Iridocorneal Endothelial Syndrome

JAMA Ophthalmology, 2014
Amir A, Azari, Mozhgan, Rezaei Kanavi, Matthew J, Thompson, Michael M, Altaweel, Heather D, Potter, Daniel M, Albert   +5 more
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[A new iridocorneal endothelial syndrome].

Klinische Monatsblatter fur Augenheilkunde, 1987
Three iridocorneal endothelial syndromes are distinguished: essential progressive iris atrophy, iris nevus (Cogan-Reese) syndrome, and Chandler's syndrome. Obviously, there are patients in whom findings do not correspond fully to any one of the three syndromes; signs and symptoms which justify being considered as a new iridocorneal endothelial syndrome
H, Slezak, M, Stur, G, Strasser
openaire   +1 more source

Management of Iridocorneal Endothelial Syndrome

Journal of Glaucoma, 1994
R, Ritch, M R, Wilson, J, Samples
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Partial Corneal Involvement in the Iridocorneal Endothelial Syndrome

American Journal of Ophthalmology, 1982
Three women (29, 31, and 38 years old) with the iridocorneal endothelial syndrome had endothelial regions with a normal-appearing cellular mosaic adjacent to endothelium with enlarged, dystrophic cells typical of this syndrome. An abrupt junction was present between the two types of endothelium. The cells in the areas with normal-appearing mosaics were
openaire   +2 more sources