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Corneal dystrophy is a group of rare hereditary disorders characterised by bilateral abnormal deposition of substances in the transparent front part of the eye called the cornea. [ 1 ] [ 2 ] [ 3 ] Signs and symptoms
Peripheral Ulcerative Keratitis (PUK) is a group of destructive inflammatory diseases involving the peripheral cornea in human eyes. [1] The symptoms of PUK include pain, redness of the eyeball, photophobia, and decreased vision accompanied by distinctive signs of crescent-shaped damage of the cornea.
As a progressive, chronic condition, signs and symptoms of Fuchs dystrophy gradually progress over decades of life, starting in middle age. Early symptoms include blurry vision upon wakening which improves during the morning, [2] as fluid retained in the cornea is unable to evaporate through the surface of the eye when the lids are closed overnight.
Keratoconus, a progressive, noninflammatory, bilateral, asymmetric disease, characterized by paraxial stromal thinning and weakening that leads to corneal surface distortion. [ 2 ] Keratoglobus , a rare noninflammatory corneal thinning disorder, characterised by generalised thinning and globular protrusion of the cornea.
There are many diseases known to cause ocular or visual changes. Diabetes , for example, is the leading cause of new cases of blindness in those aged 20–74, with ocular manifestations such as diabetic retinopathy and macular edema affecting up to 80% of those who have had the disease for 15 years or more.
Generally, diseases outlined within the ICD-10 codes H15-H19 within Chapter VII: Diseases of the eye, adnexa should be included in this category. Wikimedia Commons has media related to Disorders of sclera and cornea .
(H18.6) Keratoconus — degenerative disease: the cornea thins and changes shape to be more like a cone than a parabole (H19.3) Keratoconjunctivitis sicca — dry eyes (H20.0) Iritis — inflammation of the iris (H20.0, H44.1) Uveitis — inflammatory process involving the interior of the eye; Sympathetic ophthalmia is a subset.
[1] [2] [3] The condition occurs in predominantly middle-aged women. [ 1 ] [ 4 ] [ 3 ] Iridocorneal Endothelial (ICE) syndrome presents a unique set of challenges for both patients and ophthalmologists , and effective treatment of this group of rare ocular diseases requires a combination of diagnostic and therapeutic complexity.