Category Ophthalmology

Infectious Chorioretinal Diseases

Introduction Severe visual loss may occur among patients with infectious posterior uveitis and chorioretinitis, especially if there is a delay in the diagnosis. A number of infectious agents can affect the retinochoroidal tissue resulting in intraocular inflammation. These include a…

Vogt–Koyanagi–Harada Disease

Introduction Vogt–Koyanagi–Harada (VKH) disease is a multisystem autoimmune disease that targets melanocytes. The hallmark is bilateral granulomatous panuveitis with associated serous retinal detachments. It was first described by Alfred Vogt in Switzerland in 1906. In Japan in 1914, Yoshizo Koyanagi…

High Myopia

Introduction High myopia, defined as a spherical equivalent equal or higher than −6 diopters (D) or an axial length ≥26 mm, is one of the leading causes of low vision worldwide. The higher the myopia, the more likely complications can…

Pachychoroid

Pachychoroid Concept The term pachychoroid was first introduced by K. Bailey Freund and colleagues when describing a series of eyes showing retinal pigment epithelium (RPE) disturbances associated with an abnormally thick choroid but occurring in the absence of subretinal fluid.…

Central Serous Chorioretinopathy

Central serous chorioretinopathy (CSC) is a disorder characterized by serous retinal detachment and/or retinal pigment epithelium (RPE) detachment. These changes are usually confined to the macula but may be multifocal and more widespread. It is the fourth most common retinal…

Dystrophies

Dystrophies Retinal dystrophies include a variety of hereditary retinal disorders characterized by progressive atrophy of the retina, retinal pigment epithelium (RPE), and choriocapillaris complex. These dystrophies are generally not choroidal dystrophies, but usually retinal and/or RPE dystrophies that lead to…