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Ocular melanosis (OM) is a blue-gray and/or brown lesion of the conjunctiva that can be separated into benign conjunctival epithelial melanosis (BCEM) and primary acquired melanosis (PAM), of which the latter is considered a risk factor for uveal melanoma. [1]
Uveal melanoma is a type of eye cancer in the uvea of the eye. [4] It is traditionally classed as originating in the iris, choroid, and ciliary body, but can also be divided into class I (low metastatic risk) and class II (high metastatic risk). [4]
Generally, diseases outlined within the ICD-10 codes H10-H13 within Chapter VII: Diseases of the eye, adnexa should be included in this category. Wikimedia Commons has media related to Disorders of conjunctiva .
Nevus of Ota is a hyperpigmentation [3] that occurs on the face, most often appearing on the white of the eye. It also occurs on the forehead, nose, cheek, periorbital region, and temple. [4] It was first reported by Masao Ōta of Japan in 1939. [5]
Ocular melanosis – a condition characterized by increased pigmentation of the uveal tract, episclera, and anterior chamber angle. Oculodermal melanocytosis (nevus of Ota) [ 3 ] Pigment dispersion syndrome – a condition characterized by loss of pigmentation from the posterior iris surface which is disseminated intraocularly and deposited on ...
Side effects include eye aches, dilated pupils, headaches, nearsightedness, or blurred or dimmed vision. Macular Degeneration Medication. ... Wet macular degeneration: 10% to 15% of cases.
It is characterized by lighter pigmentation and significant effects on the eye, including decreased visual acuity and misrouting of neuronal tracks through the optic chiasm. It is due to mutation of a gene of unknown function, C10orf11 (11th uncharacterized open reading frame on chromosome 10, OMIM: 614537). [18] [20]
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