Regression of macular edema with topical brinzolamide and nepafenac alone and identification of a novel gyrate atrophy mutation.
Sign Up to like & getrecommendations! Published in 2020 at "Arquivos brasileiros de oftalmologia"
DOI: 10.5935/0004-2749.20200028
Abstract: Gyrate atrophy is a rare metabolic autosomal recessive disorder caused by ornithine aminotransferase enzyme deficiency that leads to characteristic progressive, degenerative chorioretinal findings. Patients complain mostly of low vision, night blindness, and peripheral vision loss.… read more here.
Keywords: gyrate atrophy; atrophy; brinzolamide nepafenac; topical brinzolamide ... See more keywords