Casos
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
Retinopathy of Prematurity
Retinopathy of prematurity (ROP) in adulthood can present a variety of ocular complications due to the sequelae of the disease in its acute form. Adul
Ocular ischemic syndrome
An 80-year-old male presents with floaters in both eyes.
Visual acuity is 20/25 in both eyes. Examination of the anterior segment is unremarkable. Fu
Sickle Cell Retinopathy
Sickle cell retinopathy can be present in patients with sickle cell disease, an autosomal recessive hemoglobinopathy caused by a mutation in the gene
Sickle Cell Retinopathy
Sickle cell retinopathy is a progressive vascular condition caused by intravascular hemolysis and oxygen deficiency that occurs in sickle cell disease
Acute Middle Paracentral Maculopathy
Acute Middle Paracentral Maculopathy (PAMM) is an ischemic vascular occlusion of the middle retina due to involvement of the deep vascular plexus. Amo