WAGNER'S HEREDITARY VITREORETINAL DEGENERATION
نویسندگان
چکیده
منابع مشابه
Hereditary vitreoretinal degenerations.
Developments in Ophthalmology Vol. 8 Series Editor W. Straub, Marburg a.d. Lahn KARGER S. Karger • Basel • München • Paris • London • New York• Tokyo • Sydney Hereditary Vitreoretinal Degenerations W. Lisch, Dortmund Translated by F. C. Blodi 31 figures, 5 cpl. and 1 table, 1983 KARGER S. Karger • Basel • München • Paris • London • New York • Tokyo • Sydney Developments in Ophthalmology Nationa...
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DEGENERATIONS of the retina have been known for many years and a variety of names has been applied to the various forms based in large part either on the ophthalmoscopic appearance of these lesions or on the age and mode of onset. Such terms as tapeto-retinal degeneration, primary degeneration, abiotrophy, progressive atrophy, and retinal dystrophy have been used interchangeably. However, as th...
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PURPOSE To identify the chromosomal location of the gene causing snowflake vitreoretinal degeneration (SVD), an autosomal dominant retinal degeneration characterized by small yellow-white dots in the retina, fibrillar anomaly of the vitreous humor, and retinal detachment. METHODS Clinical data were collected on 31 family members by history and examination. Thirteen family members underwent pr...
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Hereditary macular degeneration has a multifarious ophthalmoscopic appearance but is usually characterized by a sharply-defined, dense, homogenous, avascular disc resembling the intact yolk of a fried egg (Sorsby, I940; Fransois, I96I; Braley, I966). The appearance of the macula, however, may range from mild pigmentary degeneration to dense scarring with pigmentary hyperplasia. The clinical cou...
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ژورنال
عنوان ژورنال: Australian and New Zealand Journal of Ophthalmology
سال: 1980
ISSN: 0814-9763,1440-1606
DOI: 10.1111/j.1442-9071.1980.tb00885.x