Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Best's disease"'
Autor:
L. A. Katargina, E. V. Denisova, N. N. Arestova, T. B. Kruglova, N. A. Osipova, O. V. Novikova
Publikováno v:
Oftalʹmologiâ, Vol 16, Iss 1S, Pp 79-84 (2019)
Best’s disease is a relatively rare form of macular dystrophy, characterized by bilateral staged course. The cases of the choroidal neovascular membrane (XNM) formation in the course of the disease development are described, however the true freque
Externí odkaz:
https://doaj.org/article/cfc12b8edfa24f64aed83af849ea155c
Publikováno v:
Indian Journal of Ophthalmology, Vol 68, Iss 6, Pp 1173-1175 (2020)
Externí odkaz:
https://doaj.org/article/e81fefb15af849e6b059b17bde76a935
Autor:
Cristina Nieto Gómez, Lourdes de Juan-Marcos, Rebeca Lorenzo-Pérez, Álvaro Casado-Blanco, Vanesa Rivero-Gutiérrez, Emiliano Hernández-Galilea
Publikováno v:
Vision Pan-America, Vol 15, Iss 3, Pp 89-91 (2016)
Best’s Disease is a macular dystrophy characterized by a lipofuscin accumulation on the retinal pigment epithelium. Five stages have been described based on fundus examination, including choroidal neovascularization. We report a case of a 59-years
Externí odkaz:
https://doaj.org/article/ed8dadf00e0343319dd003b3a1095f64
Publikováno v:
Journal Français d'Ophtalmologie. 44:1097-1099
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88fdf0521c0ddec9c761ab485e68b7b0
https://doi.org/10.1016/j.jfo.2020.12.011
https://doi.org/10.1016/j.jfo.2020.12.011
Publikováno v:
Ophthalmic Genetics. 41:183-188
Purpose: Vitelliform Macular Dystrophy is an inherited autosomal dominant disease with variable expressivity, caused by a mutation in the BEST1 gene. We report a family with variable expressivity a...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ce64af202f7a119adf8cd3bf3d41e6d
https://doi.org/10.1080/13816810.2020.1744020
https://doi.org/10.1080/13816810.2020.1744020
Publikováno v:
Philippine Journal of Ophthalmology, Vol 35, Iss 1, Pp 36-39 (2010)
Objective: To describe a case of adult-onset foveomacular vitelliform dystrophy (AOFVD). Method: This is a case report. Results: A 22-year-old female presented with painless blurring of vision and metamorphopsia 3 days prior to consultation. Th
Externí odkaz:
https://doaj.org/article/5a50c1aeab3b40a9aa23ec543668c2d5
Publikováno v:
Indian Journal of Ophthalmology, Vol 58, Iss 2, Pp 160-162 (2010)
Best′s vitelliform macular dystrophy is a hereditary form of progressive macular dystrophy that can be complicated by choroidal neovascularization. Authors report successful treatment of choroidal neovascularization with intravitreal bevacizumab in
Externí odkaz:
https://doaj.org/article/a18ce37699a349fea41f81770c43e244
Publikováno v:
Indian Journal of Ophthalmology, Vol 68, Iss 6, Pp 1173-1175 (2020)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31fac349e9f0aacfd76e0e1f40e41dbd
http://www.ijo.in/article.asp?issn=0301-4738
http://www.ijo.in/article.asp?issn=0301-4738
Publikováno v:
Archivos de la Sociedad Española de Oftalmología (English Edition). 93:136-138
Objectives and methods Our objective is to describe a multifocal vitelliform presentation of Best's disease. The lesions in this disease may vary in size and shape, some may be a disc diameter in size, and often have some irregularity in their contou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5731ca4f9d9516f966312804bc0aca30
https://doi.org/10.1016/j.oftale.2017.08.001
https://doi.org/10.1016/j.oftale.2017.08.001
Publikováno v:
Zdravniški Vestnik, Vol 71, Iss 0 (2002)
Background. The aim of the study was to develop electrooculography in accordance with ISCEV standards and to test its accuracy in the diagnosis of Best’s disease, where the EOG results should be invariably abnormal in all affected members. The path
Externí odkaz:
https://doaj.org/article/25b54a0c278542c4932681cd301a3f46