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Cogan-Reese Syndrome
Progressive Growth of Endothelium Over Iris
Robert A. Tester;
F. Jane Durcan, MD;
Nick Mamalis, MD;
Devin C. Hymas, MD;
Paula Morris, CRA
Salt Lake City, Utah
Arch Ophthalmol. 1998;116:1126-1127.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
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A 47-YEAR-OLD woman was first diagnosed as having iridocorneal endothelial syndrome in 1988. She underwent a trabeculectomy in 1989. Photographs first taken in 1992 demonstrated some ectropian uvea and nodules covering the iris from the 7- to 3:30-o'clock positions (Figure 1 and Figure 2). Photographs taken in 1997 (Figure 3 and Figure 4) illustrate a clear progression of the nodules over previously unaffected areas of the iris.
Figure appears in full text version.
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Figure 1. Photograph taken in 1992 demonstrating nodules characteristic of the iridocorneal endothelial syndrome (Cogan-Reese variant) covering the iris from the 7- to 3:30-o'clock positions. Ectropian uvea are present from the 11- to 3:30-o'clock positions.
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Figure appears in full text version.
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Figure 2. Photograph taken in 1992 demonstrating ectropian uvea and flattened iris lacking normal stromal architecture.
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Figure appears in full text version.
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COMMENT
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