The Authors describe a clinical case of pigmented paravenous retinochoroidal atrophy in a young patient (12 years old). In the mid-peripheral area spots of accumulated pigment were observed, in particular along the veins. The exams are: funduscopy, elettroretinogram. The already examined pathology is an inherited retinic dystrophy with an uncertain transmission. According to Literature a young male case his described. Because of rarity, it is impossible describe hereditary transmission mechanism.
|Publication status||Published - Jul 2012|
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