Cogan-Reese syndrome (Q108278): Difference between revisions
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Síndrome de Cogan-Reese é uma variante clínica da síndrome iridocorneana endotelial (ICE) caracterizada por atrofia iriana variável, nódulos pigmentados e pedunculados na íris e anormalidades corneanas. Glaucoma secundário também é uma complicação comum da doença. | |||
| description / en | description / en | ||
Cogan-Reese syndrome is a clinical variant of iridocorneal endothelial (ICE) syndrome characterised by variable iris atrophy, pigmented and pedunculated nodules on the iris and corneal abnormalities. Secondary glaucoma is also a common complication of the disease. | |||
Revision as of 15:21, 17 August 2026
Cogan-Reese syndrome is a clinical variant of iridocorneal endothelial (ICE) syndrome characterised by variable iris atrophy, pigmented and pedunculated nodules on the iris and corneal abnormalities. Secondary glaucoma is also a common complication of the disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1968906450 |
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| English | Cogan-Reese syndrome |
Cogan-Reese syndrome is a clinical variant of iridocorneal endothelial (ICE) syndrome characterised by variable iris atrophy, pigmented and pedunculated nodules on the iris and corneal abnormalities. Secondary glaucoma is also a common complication of the disease. |
