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  2. Vitelliform macular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Vitelliform_macular_dystrophy

    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 .

  3. Maculopathy - Wikipedia

    en.wikipedia.org/wiki/Maculopathy

    Age-Related Macular Degeneration is a degenerative maculopathy associated with progressive sight loss. It is characterised by changes in pigmentation in the Retinal Pigment Epithelium, the appearance of drusen on the retina of the eye and choroidal neovascularization. AMD has two forms; 'dry' or atrophic/non-exudative AMD, and 'wet' or ...

  4. Macular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Macular_dystrophy

    Macular dystrophy may refer to any of these eye diseases: Macular corneal dystrophy, a rare pathological condition; Macular degeneration, or age-related macular degeneration; Vitelliform macular dystrophy, an irregular autosomal dominant eye disorder

  5. Vision disorder - Wikipedia

    en.wikipedia.org/wiki/Vision_disorder

    Diabetic Macular Edema (DME): is an eye disease specifically related to diabetes, occurring due to fluid build-up in the retina as a result of sustained high blood glucose levels. It can result in blurred vision and vision loss. [5] Eye floaters and spots: where visible cloud-like images appear to "float" in an individual's field of vision. [6]

  6. Macular degeneration - Wikipedia

    en.wikipedia.org/wiki/Macular_degeneration

    Macular degeneration, also known as age-related macular degeneration (AMD or ARMD), is a medical condition which may result in blurred or no vision in the center of the visual field. [1] Early on there are often no symptoms. [1] Over time, however, some people experience a gradual worsening of vision that may affect one or both eyes. [1]

  7. Stargardt disease - Wikipedia

    en.wikipedia.org/wiki/Stargardt_disease

    Stargardt disease is the most common inherited single-gene retinal disease. [1] In terms of the first description of the disease, [2] it follows an autosomal recessive inheritance pattern, which has been later linked to bi-allelic ABCA4 gene variants (STGD1).