Adult vitelliform macular

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Vitelliform macular dystrophyis an irregular autosomal dominant eye disorder which can cause progressive vision loss. This disorder affects the retinaspecifically cells in a small area near the center of the retina called the macula. The macula is responsible for sharp central vision, which is needed for detailed tasks such as reading, driving, and recognizing faces.

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This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed.

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Vitelliform macular dystrophy is a genetic eye disorder that can cause progressive vision loss. This disorder affects the retinathe specialized light-sensitive tissue that lines the back of the eye. Specifically, vitelliform macular dystrophy disrupts cells in a small area near the center of the retina called the macula.

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Different types of pattern dystrophies have been described throughout the 20th century by various ophthalmologist. Inbutterfly dystrophy was described by Dutch ophthalmologist August Deutman. Inworld renowned American ophthalmologist Donald Gass described adult vitelliform dystrophy as a peculiar foveomacular dystrophy which he later termed 'foveomacular vitelliform dystrophy: adult type'.

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Best vitelliform macular dystrophy BVMD is a genetic form of macular degeneration damage to a part of the eye called the macula that occurs in about 1 in 10, individuals. The condition gets worse over time, starting with blurred central vision, and possibly leading to complete loss of central vision. Peripheral vision vision from the sides of the eye and the ability of the eye to adjust to dark are unaffected.

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Adult-onset vitelliform maculopathy is a retinal disease characterized by round, yellowish deposits acquired vitelliform lesions, or AVLs found beneath the central retina or macula Figure 1. Other names used for these findings include adult pattern dystrophy and adult-onset foveomacular pigment epithelial dystrophy. Printable Fact Sheet.

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Adult-onset vitelliform maculopathy initially presents in adulthood as bilateral subtle and often asymptomatic macular lesions, which are often misdiagnosed as early age-related macular degeneration AMD. Although the prognosis is generally good with this condition, in some cases, retinal findings may progress to visually debilitating and blinding retinal pigment epithelium RPE disruption. So, in advanced cases, standard of care management should include a referral to a low vision specialist, who can improve visual function and increase quality of life for affected patients. A large, well-demarcated vitelliform lesion with underlying cuticular drusen was visible, along with sub- and intra-retinal pigment epithelium fluid accumulation, in the right eye.

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Kellner, A. Renner, S. Kohl, B.

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Macular dystrophy is a relatively rare eye condition. Linked to inherited genetic mutations, macular dystrophy causes deterioration of the most sensitive part of the central retina maculawhich has the highest concentration of light-sensitive cells photoreceptors. As the name implies, the macula of the retina is affected in macular dystrophy.

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