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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.
[3] [4] Additional symptoms may include visual impairment such as photophobia and blurred vision. Symptoms are generally worse in the mornings and patients may experience exacerbation and several remissions if left untreated. [2] It is typically caused by bacterial infection or blockage of the meibomian oil glands. [4]
In an eye examination, light-colored spots on the retina are seen. Complete loss of visual acuity may happen [ citation needed ] The name of the condition comes from the small light-colored fundus spots on the retina, scattered in a pattern like birdshot from a shotgun , but these spots might not be present in early stages.
The symptoms include poor balance and difficulty walking. Chronic cough and difficulty swallowing may also be present. Clinical findings include ataxia, sensory neuropathy, and absence of the vestibulo–ocular reflex. The syndrome was initially described in 2004. [1]
29-year-old Caitin Stickels, from Seattle, was born with Schmid-Fraccaro, also known as "Cat Eye Syndrome". The genetic disorder is known to cause an array of issues, the most visible of which ...
In 1894, Eugène Devic and his PhD student Fernand Gault described 16 patients who had lost vision in one or both eyes and within weeks developed severe spastic weakness of the limbs, loss of sensation, and often of bladder control. They recognized these symptoms were the result of inflammation of the optic nerve and spinal cord, respectively ...
Pseudoexfoliation syndrome, often abbreviated as PEX [1] and sometimes as PES or PXS, is an aging-related systemic disease manifesting itself primarily in the eyes which is characterized by the accumulation of microscopic granular amyloid-like protein fibers. [2] Its cause is unknown, although there is speculation that there may be a genetic ...
However, it may definitely be related to other diseases included in the white dot syndrome group. Acute zonal occult outer retinopathy occurs in young to middle age adults and may eventually progress to retinal cell death. Symptoms include acute visual field loss and photopsias. Suspected causes include autoimmune, viral, and fungal. [2] [5]