Corneal Donation Diseases
Corneal donation diseases encompass a spectrum of serious corneal disorders in which damage or degeneration of the cornea—the clear, dome-shaped “window” at the front of the...
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Corneal donation diseases encompass a spectrum of serious corneal disorders in which damage or degeneration of the cornea—the clear, dome-shaped “window” at the front of the...
Congenital Stationary Night Blindness (CSNB) is a group of inherited retinal disorders characterized by non‑progressive difficulty seeing in low light (nyctalopia) that begins in early childhood....
Congenital myasthenic syndromes (CMS) are a group of rare, inherited disorders of the neuromuscular junction, where communication between nerve endings and muscle fibers is impaired from...
Congenital Fibrosis of the Extraocular Muscles (CFEOM) is a rare, inherited group of eye-movement disorders present from birth. In healthy development, cranial nerves (especially the oculomotor,...
Congenital Cranial Dysinnervation Disorders (CCDDs) are a group of rare conditions present at birth in which one or more of the cranial nerves that control eye,...
A blind painful eye refers to an eye that has lost functional vision (no light perception) yet continues to experience persistent discomfort or pain. This condition...
Bestrophinopathies are a group of inherited eye disorders that affect the retina, particularly the macula—the central part responsible for sharp, detailed vision. These conditions arise due...
Batten disease, formally known as neuronal ceroid lipofuscinosis (NCL), is a group of rare, inherited neurodegenerative disorders characterized by the abnormal accumulation of autofluorescent lipopigments (lipofuscin)...
Autokeratoplasty, also known as corneal autografting, is a surgical procedure in which a patient’s own corneal tissue is transplanted to replace a damaged or opaque portion...
Anterior segment developmental anomalies (ASDAs), also known as anterior segment dysgenesis (ASD), comprise a spectrum of congenital disorders in which one or more of the front...
ADAMTSL4-related eye disorders are rare autosomal recessive conditions characterized by lens displacement (ectopia lentis), often with pupillary displacement in some cases (ectopia lentis et pupillae). The...
Acute corneal hydrops is a sudden, sight-threatening complication of corneal ectatic disorders—most commonly keratoconus—characterized by an abrupt rupture in Descemet’s membrane and endothelium. This full-thickness break...