Distrofia foveomacular viteliforme del adulto

Four cases of adult-onset foveomacular vitelliform dystrophy are shown. In two cases we were able to complete the exploration under optical coherence tomography. One of the patients developed spontaneous disappearance of the subfoveal deposit in her right eye along with an important decrease in her...

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Detalles Bibliográficos
Autores: Salinas-Alaman, A. (Ángel)|||/items/ac6c3088-aae2-4d82-97b0-d087742c1901, Sadaba-Echarri, L.M. (Luis Manuel)|||/items/f4df381d-5180-416f-b01c-67598e7d4149, Garcia-Layana, A. (Alfredo)|||/items/631fff44-be4e-42e5-ad3a-8f0f10305836
Tipo de recurso: artículo
Fecha de publicación:2003
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:español
OAI Identifier:oai:dadun.unav.edu:10171/23354
Acceso en línea:https://hdl.handle.net/10171/23354
Access Level:acceso abierto
Palabra clave:Adul-onset foveomacular vitelliform dystrophy
Optical coherence tomography
Descripción
Sumario:Four cases of adult-onset foveomacular vitelliform dystrophy are shown. In two cases we were able to complete the exploration under optical coherence tomography. One of the patients developed spontaneous disappearance of the subfoveal deposit in her right eye along with an important decrease in her visual acuity. Discussion: Adult-onset foveomacular vitelliform dystrophy is characterized by yellowish round-shaped bilateral, lesions in the subfoveal area. Optical coherence tomography reveal the presence of a slightly elevated lesion wich affects the retinal pigment epithelium and the external layers of neurosensory retina