منابع مشابه
Erythrocytic Anomalies in Hereditary Vitreo-retinal Degeneration (degeneratio Hyaloideoretinalis).
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 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...
متن کاملHereditary Glaucoma Affecting Three Generations
the ages of 50 and 60. Sindan Kia Khan had been to Col. H. Smith of Amritsar for operation and apparently an iridectomy had been done but with no improvement. I took a photograph* of the three brothers, the three old men standing behind and two of their sons sitting in front, and told them that if any of the third generation were affected to let me know at once. This year 1 discovered that a fo...
متن کاملHereditary vascular anomalies: new insights into their pathogenesis.
Increased understanding of the mechanisms of angiogenesis and lymphangiogenesis has provided a glimpse at some of the molecules involved in the pathophysiology of hemangiomas and vascular malformations. This review focuses on recent advances in our understanding of the mechanisms of angiogenesis/lymphangiogenesis and the differentiation of arterial, venous, and lymphatic vessels. We integrate t...
متن کاملHereditary macular degeneration in three generations.
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: Hereditas
سال: 2010
ISSN: 0018-0661
DOI: 10.1111/j.1601-5223.1941.tb03252.x