| Literature DB >> 21117575 |
Ioannis Emfietzoglou1, Vlassis Grigoropoulos, Pandelis Nikolaidis, George Theodossiadis, Alexandros Rouvas, Panagiotis Theodossiadis.
Abstract
A patient with cone-rod dystrophy, who was examined thoroughly with biomicroscopy, fluorescein angiography, optical coherence tomography, and electrophysiology, is presented. Although fluorescein angiography depicted only window-defect type of hyperfluorescence, optical coherence tomography disclosed detachment of the neurosensory retina, focal absence of the outer parts of the photoreceptors' layer in the fovea, and cystoid edema in the macula. To the authors' knowledge, these findings have not been described in cone-rod dystrophy so far. Copyright 2010, SLACK Incorporated.Entities:
Mesh:
Year: 2010 PMID: 21117575 DOI: 10.3928/15428877-20101124-10
Source DB: PubMed Journal: Ophthalmic Surg Lasers Imaging ISSN: 1542-8877