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Most cases of recurrent corneal erosion are acquired. There is often a history of recent corneal injury, such as corneal abrasion or ulcer, but also may be idiopathic or due to corneal dystrophy or corneal disease. In other words, one may develop corneal erosions as a result of another disorder, such as epithelial basement membrane dystrophy ...
Corneal abrasions are also a common and recurrent feature in people with specific types of corneal dystrophy, such as lattice corneal dystrophy. Lattice dystrophy gets its name from an accumulation of amyloid deposits, or abnormal protein fibers, throughout the middle and anterior stroma.
Corneal Abrasion Eye Drops. Corneal abrasions are a common eye problem in which the eye's cornea (an important part of the eye that allows light to enter properly) is scratched. In order to treat ...
Epithelial basement membrane dystrophy (EBMD) is a disorder of the eye that can cause pain and dryness.EBMD, also known as map-dot-fingerprint dystrophy and Cogan microcystic epithelial dystrophy, is a corneal epithelial disease that may result in recurrent corneal erosions, irregular corneal astigmatism, and decreased vision.
Congenital stromal corneal dystrophy; Cornea verticillata; Corneal abrasion; Corneal dystrophy; ... Recurrent corneal erosion;
Due to the different underlying causes, proper diagnosis, treatment, and prognosis can only be determined by an eye care professional. Punctate epithelial erosions may be treated with artificial tears.
Corneal ulcer, also called keratitis, is an inflammatory or, more seriously, infective condition of the cornea involving disruption of its epithelial layer with involvement of the corneal stroma. [ 1 ] [ 2 ] [ 3 ] It is a common condition in humans particularly in the tropics and in farming. [ 4 ]
Reis-Bücklers corneal dystrophy is a disease of the eye, a rare corneal dystrophy of unknown cause, in which the Bowman's layer of the cornea undergoes disintegration. The disorder is inherited in an autosomal dominant fashion, and is associated with mutations in the gene TGFB1 .