منابع مشابه
Erythrocytes in Vitreo-retinal Degeneration
Two hereditary syndromes characterized by the association of retinal changes and erythrocytic anomalies have been described: (1) Retinopathy complicating haemoglobin anomalies, thalassaemia (Rudd, Evans, and Peeney, 1953), or sickle-cell anaemia (Lieb, Geeraets, and Guerry, 1959); (2) Atypical retinitis pigmentosa with thorny erythrocytes (acanthocytosis: Bassen and Kornzweig, 1950; Kornzweig a...
متن کامل23-gauge sutureless vitreo-retinal surgery for superior rhegmatogenous retinal detachment.
OBJECTIVE To determine the results of 23-gauge sutureless vitreo-retinal surgery for superior/supero-temporal rhegmatogenous retinal detachment (RRD). STUDY DESIGN Quasi experimental study. PLACE AND DURATION OF STUDY LRBT, Free Base Eye Hospital, Karachi, from January 2010 to December 2011. METHODOLOGY Adult patients who underwent 23-gauge sutureless vitreo-retinal surgery along with use...
متن کاملNew approach in training in East Africa: vitreo-retinal surgery from 2000 to 2007 in Kenya.
From an estimated total of 37 million blinds worldwide, a vastly over-proportional share of seven million is living in Africa. 2 Most causes of blindness in developing countries are relatively easy to cure, provided minimally adequate medical resources are available, resulting in an evident demand for ophthalmologic measures particularly in Sub-Saharan Africa. Therefore, the WHO has initiated a...
متن کاملAdvances in Vitreo-retinal Surgery: 23-gauge Sutureless Pars Plana Vitrectomy
Pars plana vitrectomy is one of the most common surgical procedures performed for the treatment of various vitreo-retinal diseases such as retinal detachment, vitreous haemorrhage, proliferative diabetic retinopathy, epiretinal membrane and macular hole. Traditionally, most vitrectomy surgical systems utilise the 20-gauge instruments pars plana vitrectomy includes multiple incisions including p...
متن کاملErythrocytic Anomalies in Hereditary Vitreo - Retinal Degeneration ( Degeneratio Uiyaloideoretinalis )
Two hereditary syndromes characterized by the association of retinal changes and erythrocytic anomalies have been described: (1) Retinopathy complicating haemoglobin anomalies, thalassaemia (Rudd, Evans, and Peeney, 1953), or sickle-cell anaemia (Lieb, Geeraets, and Guerry, 1959); (2) Atypical retinitis pigmentosa with thorny erythrocytes (acanthocytosis: Bassen and Kornzweig, 1950; Kornzweig a...
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ژورنال
عنوان ژورنال: Graefe's Archive for Clinical and Experimental Ophthalmology
سال: 2005
ISSN: 0721-832X,1435-702X
DOI: 10.1007/s00417-005-0012-9