Familial Hyaline Dystrophy in the Fundus Oculi or Doyne's Family Honeycomb "choroiditis".
نویسنده
چکیده
منابع مشابه
Doyne's honeycomb retinal degeneration. Clinical and genetic features.
IN 1899 Doyne described a fundus condition which he had observed in four sisters. The ophthalmoscopic appearance was of closely-grouped white spots involving the disc-macular area in a pattern he termed "Honeycomb". He believed the lesions were probably due to an exudate in the choroid, and therefore called the condition honeycomb choroiditis (Doyne, 1910), although it was shown shortly afterwa...
متن کاملPolypoidal choroidal vasculopathy associated with Doyne's familial choroiditis: treatment with thermal laser.
PURPOSE To report the unusual occurrence of polypoidal choroidal vasculopathy (PCV) in a patient with Doyne's familial honeycomb choroiditis (DFHC) and its course after laser treatment. DESIGN Interventional case report. METHODS Indocyanine green (ICG) angiography guided laser was performed on active polypoidal lesions. RESULTS A 45-year-old man with a 15-year history of bilateral DFCH an...
متن کاملFundus dystrophy with unusual features; a histological study.
IN an earlier communication (Sorsby and Mason, 1949), an account was given of a fundus dystrophy observed in five families, which showed onset at about the age of 40, dominant inheritance, and a progressive course. The earliest ophthalmoscopical reactions in this affection are a central retinal lesion showing oedema, haemorrhage, and exudates. Subsequently, there is considerable scarring, with ...
متن کاملCurvilinear pigmentary lesions in a rod-cone dystrophy.
PURPOSE To report a peculiar curvilinear pigmentary lesion in the peripheral fundus in a rod-cone dystrophy. METHODS Observational case report. Fundus examination of a 57-year-old woman who was known to have a generalized rod-cone dystrophy since she was 8 years old. RESULTS The peripheral fundus examination revealed a curvilinear lesion which resembles a well-known finding associated with ...
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We report a case of birdshot chorioretinopathy (BSCR) in a patient with facioscapulohumeral muscular dystrophy (FSHD). A 40-year-old male with history of facioscapulohumeral muscular dystrophy with significant facial diplegia and lagophthalmos presents for an evaluation of bilateral choroiditis with vasculitis and optic disc edema. Clinical examination included fundus and autofluorescence photo...
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ورودعنوان ژورنال:
- The British journal of ophthalmology
دوره 21 2 شماره
صفحات -
تاریخ انتشار 1937