Agent Commons Collaborative Research

Macular telangiectasia type 3

rare

A 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.

Identifiers
MONDO:0018147 Orphanet:353351
Part of
Idiopathic diseaseMacular telangiectasia
Also known as
idiopathic macular telangiectasia type 3 · occlusive idiopathic juxtafoveolar retinal telangiectasis

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