Casos
Pattern Dystrophy – Multifocal Pattern
A 65-year-old male comes in for a check-up.
VA OD 20/20 OS 20/20.
In the fundus examination, multiple small yellowish lesions are observed scattered
Adult-Onset Foveomacular Vitelliform Dystrophy
35-year-old male who comes in for a checkup.
VA OD 20/20 OS 20/20.
Fundus examination reveals a rounded yellowish lesion at the foveal level in both
Adult-Onset Foveomacular Vitelliform Dystrophy
It is characterized by the presence of rounded, bilateral, yellowish lesions with subfoveal localization. The vitelliform lesions are mainly composed
Butterfly-Shaped Macular Dystrophy
Pattern macular dystrophies are a group of autosomal dominant macular diseases characterized by various patterns of pigment deposits in the macula. Am
Adult-Onset Foveomacular Vitelliform Dystrophy
Adult-onset foveomacular vitelliform dystrophy is characterized by bilateral, rounded, yellowish lesions at the macular level, with an appearance simi
Central Areolar Choroidal Dystrophy
A 45-year-old woman comes in for a check-up.
VA OD 20/400 OS 20/200.
In the fundus, central retinal atrophy with pigment deposition and visualizatio
Choroideremia
11-year-old male patient comes for a check-up.
VA OD 20/20 OS 20/25.
The fundus examination shows severe chorioretinal atrophy both in the periphery
Cone Dystrophy
Cone dystrophies represent a heterogeneous group with more than 25 identified causative genes.
The onset of symptoms usually occurs from adolescence,
Achromatopsia
Achromatopsia is a stationary congenital defect characterized by selective dysfunction of the cone system. It is a rare congenital disease of genetic








