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Macular telangiectasia type 3
MONDO:0018147A rare, acquired, macular telangiectasia characterized by progressive visual loss, due to bilateral juxtafoveolar capillary occlusions, capillary telangiectasia, and minimal exudation. It is associated with systemic or cerebral vascular occlusive disease.
Also known as: idiopathic macular telangiectasia type 3, occlusive idiopathic juxtafoveolar retinal telangiectasis
0 clinical trials for this condition and its sub-types, 0 tagged with Macular telangiectasia type 3 itself.
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