can deteriorate, and subretinal neovascular membranes, macular detachment, and central serous retinopathy can develop.

Type III

Type III is very rare, it is characterized by a mixture of subepithelial and subendothelial immune and/or complement deposits. These deposits elicit an immune response, causing damage to cells and structures within their vicinity. Has similar pathological findings of Type I disease.

A candidate gene has been identified on chromosome 1.

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