Relentless Placoid Chorioretinitis
White dot syndrome
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Ara
Central Areolar Choroidal Dystrophy (CACD)
Hereditary disease of the choroid
Combined choroidal neovascularization
Combined type 1 and type 2 choroidal neovascularisation in armd
Sympathetic ophthalmia
Posttraumatic uveitis
BALAD
Bacillary layer detachment, extensive changes in structure of the retina
Retinal Angiomatous Proliferation (RAP)
neovascularisation in the retina, armd
Peripapillary Choroidal Neovascularisation
Choroidal neovascularisation originating from the peripapillary region
Subfoveal Choroidal Neovascular Membrane
Armd with choroidal neovascularisation underneath the fovea.
Juxtafoveal Chorodial Neovascular Membrane
Choroidal neovascularisation adjacent to foveal region
Type 1 Neovascularisation
Most frequently encountered choroidal neovascularisation type in armd
Idiopathic Polypoidal Choroidal Vasculopathy
A rare subtype of armd, there are more cases diagnosed in recent years.
Vascularized Pigment Epithelial Detachment
May be accepted as precursor findings of choroidal neovascularisation
Pigment Epithelial Detachment
Mostly encountered in armd but other etiologies must be considered in differential diagnosis
Retinal Pigment Epithelial Tears
A rare but devastating complication of both the disease itself and treatment in armd.
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