File:Vogt.gif
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English: The patient was a 12-year-old male with a clinical diagnosis of Spielmeyer-Vogt disease. He was first seen at age five years with a symptom of severe visual disability with vision light perception only. An examination of the retina revealed a pepper-type fundus, somewhat granular with a normal optic nerve, but no foveal reflex. By age seven years the patient was severely mentally retarded and was hospitalized with convulsive episodes. He died about two months later. A gross examination of the posterior portion of the eye revealed marked optic atrophy |
Date | Unknown date |
Source | [1] |
Author | National Eye Institute |
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public domain |
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current | 15:07, 10 June 2008 | 708 × 560 (280 KB) | Filip em (talk | contribs) | {{Information |Description={{en|1=The patient was a 12-year-old male with a clinical diagnosis of Spielmeyer-Vogt disease. He was first seen at age five years with a symptom of severe visual disability with vision light perception only. An examination of |
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