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Rev. bras. oftalmol ; 70(3): 185-187, maio-jun. 2011. ilus
Article in Portuguese | LILACS | ID: lil-596345

ABSTRACT

RESUMO O objetivo deste relato é descrever um caso de síndrome iridocorneana endotelial, na variante clínica atrofia essencial de íris, com concomitante hipertrofia congênita do epitélio pigmentar da retina no mesmo olho.


The aim of this report is to describe a case of iridocornel endothelial syndrome with the clinical variant essential iris atrophy, which presents concomitant congenital hypertrophy of the retinal pigment epithelium in the same eye.

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