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Fundus of geographic atrophy. Geographic atrophy (GA), also known as atrophic age-related macular degeneration (AMD) or advanced dry AMD, is an advanced form of age-related macular degeneration that can result in the progressive and irreversible loss of retinal tissue (photoreceptors, retinal pigment epithelium, choriocapillaris) which can lead to a loss of central vision over time.
Retinal tufts increase the risk of a retinal tear or a detached retina, although the risk is not high- 1% of tufts are thought to lead to retinal detachment. [ 2 ] [ 6 ] In addition if there is retinal thinning near a zonular traction tuft, there is an increased risk of retinal detachment.
It most commonly occurs in people over the age of fifty and in the United States is the most common cause of vision loss in this age group. [1] [3] About 0.4% of people between 50 and 60 have the disease, while it occurs in 0.7% of people 60 to 70, 2.3% of those 70 to 80, and nearly 12% of people over 80 years old. [3]
Aqueous cells without the signs of uveitis, elevated intraocular pressure and rhegmatogenous retinal detachment with tears around the ora serrata are the main signs of Schwartz–Matsuo syndrome. [1] Intra ocular pressure can be as high as 60–70 mm Hg and is responsive to aqueous suppressants. [ 3 ]
Usually, this happens slowly over time and does not cause any symptoms, and medical intervention is neither needed nor recommended. Sometimes other retinal problems (such as tears, breaks, or holes) may be present along with lattice degeneration. However, these problems may also be distinct from or independent of lattice degeneration itself.
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).
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.
Multiple evanescent white dot syndrome occurs mostly in females. Symptoms include a sudden loss of central vision, but patients eventually regain normal vision. The white dots are small and located in the posterior pole at the level of the retinal pigment epithelium. The white dots may disappear after the first few weeks of the disease.