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Frequency. 60 million (2015) [6] A cataract is a cloudy area in the lens of the eye that leads to a decrease in vision of the eye. [1] [7] Cataracts often develop slowly and can affect one or both eyes. [1] Symptoms may include faded colours, blurry or double vision, halos around light, trouble with bright lights, and difficulty seeing at night ...
At some point—usually as you enter middle age—most people develop this eye condition, which is a clouding of the eye’s lens that can get progressively worse and impair your vision. According ...
Reactive arthritis. Rheumatoid arthritis. Ehlers-Danlos Syndrome. Sarcoidosis. Scleroderma. Systemic lupus erythematosus. Temporal arteritis. Relapsing polychondritis. Granulomatosis with polyangiitis 50-60% have ophthalmologic manifestations, which can be a presenting feature in a minority of patients.
H15-H22 Disorders of sclera, cornea, iris and ciliary body. (H15.0) Scleritis — a painful inflammation of the sclera. (H16) Keratitis — inflammation of the cornea. (H16.0) Corneal ulcer / Corneal abrasion — loss of the surface epithelial layer of the eye's cornea. (H16.1) Snow blindness / Arc eye — a painful condition caused by exposure ...
Uveitis. Uveitis ( / ˌjuːvi.aɪtɪs /) is inflammation of the uvea, the pigmented layer of the eye between the inner retina and the outer fibrous layer composed of the sclera and cornea. [1] The uvea consists of the middle layer of pigmented vascular structures of the eye and includes the iris, ciliary body, and choroid.
Oculocerebrorenal syndrome (also called Lowe syndrome) is a rare X-linked recessive disorder characterized by congenital cataracts, hypotonia, intellectual disability, proximal tubular acidosis, aminoaciduria and low-molecular-weight proteinuria.
List of autoimmune diseases. Dermatosis in Crohn's disease. Demyelination in MS. PAS stain of lupus nephritis. Autoimmune urticaria. Proptosis in Graves' disease. This article provides a list of autoimmune diseases. These conditions, where the body's immune system mistakenly attacks its own cells, affect a range of organs and systems within the ...
Werner syndrome has an autosomal recessive pattern of inheritance. Werner syndrome (WS) or Werner's syndrome, also known as "adult progeria ", [1] is a rare, autosomal recessive disorder [2] which is characterized by the appearance of premature aging. [3] Werner syndrome is named after the German scientist Otto Werner. [4]
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