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KMID : 0360219760170030347
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Journal of the Korean Ophthalmological Society
1976 Volume.17 No. 3 p.347 ~ p.351
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Retinitis Punctata Albescens
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Abstract
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Two cases of Retinitis Punctata Albescens are presented. One case occurred in two successive generations without a history of consanguity and is suspected strongly a dominant form of heredity which has been reported for the first time in Korea, and is probably a progressive type for its clinical signs and symptoms.
The other case; is stationary type of albipunctate dystrophy and is inherited in usual recessive form of heredity.
In both cases, there were fundus changes characterized by a powdering with white discrete dots beneath the retinal vessels, raised threshold in dark adaptation and other typical signs.
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