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Combined central retinal artery and vein occlusion; first manifestation of lupus in a pediatric patient.
Arch Soc Esp Oftalmol (Engl Ed)
March 2019
Departamento de Retina y Vítreo, Hospital General de México «Dr. Eduardo Liceaga», Ciudad de México, Estados Unidos Mexicanos. Electronic address:
Combined central retinal artery and vein occlusion is uncommon in adults and even more so in young people. The main origins are vasculitis and thromboembolic disorders. The prognosis is poor due to irreversible visual loss and the development of neovascular glaucoma (NVG).
View Article and Find Full Text PDFAtypical chorioretinal coloboma in a Golden Retriever: a retinographic, fluoroangiographic, and optical coherence tomography study.
Vet Ophthalmol
November 2016
Clinica Veterinaria Oftalmológica Ocaña, C/de Ocaña n° 201, 28047, Madrid, Spain.
Purpose: To report a case of canine atypical chorioretinal coloboma where ophthalmoscopic, fluoroangiographic and optical coherence tomography characteristics are described.
Animal Studied: A 2-year-old Golden Retriever dog in which routine ophthalmoscopic examination allowed diagnosis of a posterior coloboma on the left eye.
Procedures: Retinography, fluorescein angiography, and optical coherence tomography were performed to characterize the lesion of the left fundus.
Fractal analysis of fluoroangiographic patterns in anterior ischaemic optic neuropathy and optic neuritis: a pilot study.
Clin Exp Ophthalmol
May 2008
Departments of Ophthalmology and Neurosurgery, University of Siena, Siena, Italy.
Background: To evaluate by means of fractal analysis the vascular pattern of the optic nerve head obtained by fluorescein angiogram, in non-arteritic anterior ischaemic optic neuropathy (NAION) and optic neuritis (ON).
Methods: Twenty-nine patients at the Department of Ophthalmology of the University of Siena, diagnosed as having either NAION or ON by clinical and instrumental criteria, were prospectively subjected to fractal analysis: 11 patients with NAION and 18 patients with ON. In the ON group, 12 patients showed optic disc oedema, whereas six patients showed no optic disc oedema.
Congenital macular macrovessels.
Graefes Arch Clin Exp Ophthalmol
September 2006
Department of Ophthalmology, University Federico II, Via Pansini 5, 80131, Naples, Italy.
Background: Congenital aberrant macular vessels are rare and may cause visual impairment when crossing the fovea, when causing the formation of foveolar cysts, or when haemorrhage occurs.
Methods: From the records of patients with vascular anomalies seen at the Retina Department of the University Federico II in Naples from 1980 to 2005, we reviewed all cases presenting an abnormal, large, retinal vessel crossing the macular region.
Results: An anomalous macular macrovessel was present in 13 cases.
[Best's vitelliform dystrophy with complications of a neovascular membrane and hemorrhage].
Cesk Slov Oftalmol
May 2002
Ocní klinika VFN a 1. LF UK, Praha.
Unlabelled: The objective of the paper is to draw attention to an uncommon picture of Best s vitelliform dystrophy of the macula (BVD) complicated by a choroidal neovascular membrane (CNVM) and haemorrhage. In an 8-year-old boy where incidentally at the age of 5 years cystic changes in both maculars were found and a reduced central visual acuity (CVA) of the left eye, the CVA of the so far asymptomatic right eye suddenly deteriorated. In the right macula a vitelliform focus was present the lower half of which was formed by a vascularized scar with subretinal haemorrhage on the margin.
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