No abstract available
Plain language summary
This case report describes a diagnosis of presumed autoimmune pigmented paravenous retinochoroidal atrophy in a 69-year-old patient who presented with slowly progressive vision loss and nyctalopia.
MeSH terms
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Atrophy*
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Autoimmune Diseases*
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Eye Diseases, Hereditary*
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Female
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Humans
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Retinal Degeneration*
Supplementary concepts
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Pigmented Paravenous Chorioretinal Atrophy