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There is no cure, but pigmentary glaucoma can be managed with eye drops or treated with simple surgeries. If caught early and monitored, chances of glaucoma are greatly reduced. A 2016 Cochrane Review sought to determine the effectiveness of YAG laser iridotomy versus no laser iridotomy for pigment dispersion syndrome and pigmentary glaucoma ...
Nd:YAG laser peripheral iridotomy (LPI) may be used in patients susceptible to or affected by angle closure glaucoma or pigment dispersion syndrome. During laser iridotomy, laser energy is used to make a small, full-thickness opening in the iris to equalize the pressure between the front and back of the iris, thus correcting any abnormal ...
Generally, diseases outlined within the ICD-10 codes H00-H59 within Chapter VII: Diseases of the eye, adnexa should be included in this category. Wikimedia Commons has media related to Diseases and disorders of the eye and adnexa .
Pigment dispersion syndrome – a condition characterized by loss of pigmentation from the posterior iris surface which is disseminated intraocularly and deposited on various intraocular structures, including the anterior surface of the iris. [medical citation needed]
Skin pigmentation is a frequent disorder that has a number of potential causes. Genetics, sun exposure, and some drugs are the three main factors that contribute to skin pigmentation.
During gonioscopy (where the structures of the eye's anterior segment are examined), if an abundance of brown pigment is seen at or anterior to Schwalbe's line, a Sampaolesi line is said to be present. [1] [2] [3] The presence of a Sampaolesi line can signify pigment dispersion syndrome or pseudoexfoliation syndrome. [4] [5]
Those with moderate amounts of myopia are more likely to have pigment dispersion syndrome or pigmentary glaucoma. [84] High myopia usually describes myopia of −6.00 or more. [65] [85] People with high myopia are more likely to have retinal detachments [86] and primary open angle glaucoma. [87]
Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is an acquired inflammatory uveitis that belongs to the heterogenous group of white dot syndromes in which light-coloured (yellowish-white) lesions begin to form in the macular area of the retina.