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Vitelliform macular dystrophy is an irregular autosomal dominant eye disorder which can cause progressive vision loss. [1] This disorder affects the retina , specifically cells in a small area near the center of the retina called the macula .
Generally, diseases outlined within the ICD-10 codes H30-H36 within Chapter VII: Diseases of the eye, adnexa should be included in this category. Wikimedia Commons has media related to Disorders of choroid and retina .
(H35.3) Age-related macular degeneration — the photosensitive cells in the macula malfunction and over time cease to work (H35.3) Macular degeneration — loss of central vision, due to macular degeneration Bull's Eye Maculopathy (H35.3) Epiretinal membrane — a transparent layer forms and tightens over the retina (H35.4) Peripheral retinal ...
Monofixation syndrome (MFS) (also: microtropia or microstrabismus) is an eye condition defined by less-than-perfect binocular vision. [1] It is defined by a small angle deviation with suppression of the deviated eye and the presence of binocular peripheral fusion. [2]
Bietti's crystalline dystrophy (BCD) is a rare autosomal recessive [2] eye disease named after G. B. Bietti. [ 3 ] BCD is a rare disease and appears to be more common in people with Asian ancestry.
Birdshot chorioretinopathy, now commonly named birdshot uveitis or HLA-A29 uveitis, [1] is a rare form of bilateral posterior uveitis affecting both eyes.It causes severe, progressive inflammation of both the choroid and retina.
Coats' disease is a rare extramuscular manifestation of facioscapulohumeral muscular dystrophy (FSHD). A single study reported it in 1 percent of FSHD patients, most often those with FSHD type 1 (FSHD1) with large D4Z4 deletions. [4]
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.