Casos
Multiple Evanescent White Dot Syndrome (MEWDS)
MEWDS is a rare entity of unknown etiology that typically affects young women. The most characteristic finding in the fundus is the presence of multip
Familial Exudative Vitreoretinopathy (FEVR)
Familial Exudative Vitreoretinopathy (FEVR) is a group of inherited retinal disorders characterized by abnormal retinal angiogenesis, leading to incom
Methylmalonic Acidemia with Homocystinuria Type CbLC
Methylmalonic acidemia with homocystinuria is a congenital error in metabolism, consisting of an inability to convert vitamin B12 (cobalamin) into its
Retinal dystrophy associated with mutation in the HK1 gene
Retinitis pigmentosa is a diffuse and hereditary retinal dystrophy that affects photoreceptors, initially rods and later cones (rod-cone dystrophy). T
Posterior Vitreous Detachment
Posterior vitreous detachment is the process by which the posterior hyaloid partially or completely separates from the retina. In most cases, it does
X-linked juvenile retinoschisis
X-linked retinoschisis (XLRS) is a vitreoretinal degeneration caused by various mutations in the RS1 gene. It predominantly affects males and usually
Stargardt Disease
67-year-old woman who comes for a check-up.
VA OD 20/100 OS 20/20.
In the fundus of both eyes, yellowish deposits (flecks) are observed in the poste
Stargardt Disease
Currently, fundus flavimaculatus (FF) and Stargardt Disease (SD) are terms that can be used to name a heterogeneous group of hereditary retinal disord
Best Disease
A 38-year-old male presents with progressive vision loss over the past few months.
VA OD 20/25 OS 20/25.
Fundus examination reveals a bilateral macu