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Choroideremia (/ k ɒ ˌ r ɔɪ d ɪ ˈ r iː m i ə /; CHM) is a rare, X-linked recessive form of hereditary retinal degeneration that affects roughly 1 in 50,000 males. The disease causes a gradual loss of vision, starting with childhood night blindness, followed by peripheral vision loss and progressing to loss of central vision later in life.
In PCV, sudden blurring of vision or a scotoma in the central field of vision may occur in one or both eyes. [2] Another symptom is metamorphopsia. [1] Signs include polypoidal lesions, orange-red lesions in fundus, subretinal fluid, retinal detachment, subretinal hemorrhages, subretinal fibrinous material, hard exudates and drusen. [1]
The Macular Society is a UK [1] [2] charity that offers support to anyone affected by central vision loss.. Many of the charity's members have age-related macular degeneration (AMD), but its services are open to people with various retinal conditions, including myopic macular degeneration, diabetic retinopathy, and inherited retinal dystrophies like Stargardt disease, Best disease, and Sorsby ...
For patients suffering from macular degeneration in the intermediate stage and advanced stages, this takes away people’s ability to read their own medications, do their own finances and their ...
In 2012, the Oscar winner shared that she’d been diagnosed with the eye condition macular degeneration, which is the most common cause of vision loss in people 50 and older, according to Johns ...
Recently, central serous chorioretinopathy has been understood to be part of the pachychoroid spectrum. [5] [6] In pachychoroid spectrum disorders, of which CSR represents stage II, the choroid, the highly vascularized layer below the retina, is thickened and congested with increased blood vessel diameter, especially in the deep choroid (the so-called Haller's layer).
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