Iridocorneal endothelial syndrome (Q106038): Difference between revisions

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Síndrome iridocorneana endotelial (ICE) descreve um grupo de endoteliopatias corneanas proliferativas progressivas que compreende a síndrome de Chandler, a síndrome Cogan-Reese e a atrofia essencial da íris (veja estes termos), que afeta principalmente mulheres adultas jovens e se caracteriza por atrofia e buracos irianos, distorção pupilar, sinéquias anteriores, edema corneano e frequentemente com complicações como glaucoma secundário e descompensação corneana.
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Iridocorneal endothelial (ICE) syndrome describes a group of progressive corneal proliferative endotheliopathies comprised of Chandler s syndrome, Cogan-Reese syndrome and essential iris atrophy (see these terms), affecting mainly young adult females and characterised by iris holes and atrophy, papillary distortion, anterior synechiae, corneal oedema and often with secondary glaucoma and corneal decompensation as complications

Revision as of 12:48, 17 August 2026

Iridocorneal endothelial (ICE) syndrome describes a group of progressive corneal proliferative endotheliopathies comprised of Chandler s syndrome, Cogan-Reese syndrome and essential iris atrophy (see these terms), affecting mainly young adult females and characterised by iris holes and atrophy, papillary distortion, anterior synechiae, corneal oedema and often with secondary glaucoma and corneal decompensation as complications
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    Iridocorneal endothelial syndrome
    Iridocorneal endothelial (ICE) syndrome describes a group of progressive corneal proliferative endotheliopathies comprised of Chandler s syndrome, Cogan-Reese syndrome and essential iris atrophy (see these terms), affecting mainly young adult females and characterised by iris holes and atrophy, papillary distortion, anterior synechiae, corneal oedema and often with secondary glaucoma and corneal decompensation as complications

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