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Toxic anterior segment syndrome is an acute, sterile anterior segment inflammation following generally uneventful cataract and anterior segment surgery. [ 1 ] One of the main factors in differentiating toxic anterior segment syndrome from an infectious endophthalmitis is the rapid onset.
Thygeson's superficial punctate keratopathy (TSPK) is a disease of the eyes.The causes of TSPK are not currently known, but details of the disease were first published in the Journal of the American Medical Association in 1950 by American ophthalmologist Phillips Thygeson (1903–2002), after whom it is named.
Measurements of tear osmolarity may be beneficial in diagnosing concurrent dry eye syndrome (DES), which may be responsible for overlapping symptoms and would allow the physician to decipher between conditions and move forward with the most beneficial protocol for the patient.
Another treatment that is sometimes suggested is lacrimal plugs that prevent tears from draining from the surface of the eye. Dry eye syndrome is a common eye disease. [3] It affects 5–34% of people to some degree depending on the population looked at. [5] Among older people it affects up to 70%. [10] In China it affects about 17% of people. [11]
Leber's hereditary optic neuropathy (LHON) is a mitochondrially inherited (transmitted from mother to offspring) degeneration of retinal ganglion cells (RGCs) and their axons that leads to an acute or subacute loss of central vision; it predominantly affects adult males, and onset is more likely in younger adults.
Blepharospasm may occur as secondary to conditions including dry eyes and other specific ocular disease or conditions, Meige's syndrome and other forms of dystonia, and Parkinson's disease and other movement disorders. [3] Blepharospasm occurs in middle age and is more frequent among women than men.
Giant cell arteritis: Giant cell arteritis can result in granulomatous inflammation within the central retinal artery and posterior ciliary arteries of eye, resulting in partial or complete occlusion, leading to decreased blood flow manifesting as amaurosis fugax. Commonly, amaurosis fugax caused by giant cell arteritis may be associated with ...
Adie syndrome, also known as Holmes–Adie syndrome, is a neurological disorder characterized by a tonically dilated pupil that reacts slowly to light but shows a more definite response to accommodation (i.e., light-near dissociation). [1] It is frequently seen in females with absent knee or ankle jerks and impaired sweating.