2005
DOI: 10.1590/s0004-27492005000200021
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Fundus flavimaculatus e neovascularização subretiniana: relato de caso

Abstract: Fundus flavimaculatus is a progressive, bilateral, hereditary retinal dystrophy characterized by ill-defined, yellowish, pisiform flecks at the level of the retinal pigment epithelium. Since the disease process is at level of the retinal pigment epithelium, it is not surprising that subretinal macular neovascularizations might occur. Nevertheless, they have been rarely reported as complications of the disease. The following report describes a case of fundus flavimaculatus that progressed with blurred vision by… Show more

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Cited by 3 publications
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“…Stargardt Disease is one of the causes that lead to low vision, a progressive retinal dystrophy, hereditary autosomal recessive, usually bilateral that starts in the first two decades of life 3 . Stargardt Disease has a population incidence estimated from 1/1660 to 1/15000 and is responsible for about 7% of retinal abnormalities found in the world.…”
Section: Conflict Of Interest: Non-existentmentioning
confidence: 99%
“…Stargardt Disease is one of the causes that lead to low vision, a progressive retinal dystrophy, hereditary autosomal recessive, usually bilateral that starts in the first two decades of life 3 . Stargardt Disease has a population incidence estimated from 1/1660 to 1/15000 and is responsible for about 7% of retinal abnormalities found in the world.…”
Section: Conflict Of Interest: Non-existentmentioning
confidence: 99%