Literature DB >> 21117575

Optical coherence tomography findings in a case of cone-rod dystrophy.

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.

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Year:  2010        PMID: 21117575     DOI: 10.3928/15428877-20101124-10

Source DB:  PubMed          Journal:  Ophthalmic Surg Lasers Imaging        ISSN: 1542-8877


  2 in total

1.  Multimodal imaging of foveal cavitation in retinal dystrophies.

Authors:  Maurizio Battaglia Parodi; Maria Vittoria Cicinelli; Pierluigi Iacono; Gianluigi Bolognesi; Francesco Bandello
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2016-08-05       Impact factor: 3.117

2.  Morphologic characteristics of the outer retina in cone dystrophy on spectral-domain optical coherence tomography.

Authors:  Soo Chang Cho; Se Joon Woo; Kyu Hyung Park; Jeong-Min Hwang
Journal:  Korean J Ophthalmol       Date:  2013-01-15
  2 in total

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