When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  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. Bestrophin 1 - Wikipedia

    en.wikipedia.org/wiki/Bestrophin_1

    Adult-onset vitelliform macular dystrophy (AVMD) consists of lesions similar to BVMD on the retina. However, the cause is not as definitive as BVMD. The inability to diagnosis AVMD via genetic testing makes differentiating between AVMD and pattern dystrophy difficult.

  4. Macular degeneration - Wikipedia

    en.wikipedia.org/wiki/Macular_degeneration

    Vitelliform macular dystrophy Sorsby's fundus dystrophy is an autosomal dominant, retinal disease characterized by sudden acuity loss resulting from untreatable submacular neovascularisation

  5. Macular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Macular_dystrophy

    Vitelliform macular dystrophy, an irregular autosomal dominant eye disorder This page was last edited on 29 December 2019, at 07:48 (UTC). Text is available under ...

  6. Geographic atrophy - Wikipedia

    en.wikipedia.org/wiki/Geographic_atrophy

    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.

  7. Vascular anomaly - Wikipedia

    en.wikipedia.org/wiki/Vascular_anomaly

    Usually, it is present at birth as a flat, reddish-purple, tense and edematous lesion. Although half of lesions are congenital, 58% of KHE develop during infancy, 32% between age 1 and 10 years (32%) and 10% after 11 years of age. Moreover, adult onset has been described too with mainly males being affected. Both sexes are affected equally in ...

  8. Sickle cell retinopathy - Wikipedia

    en.wikipedia.org/wiki/Sickle_cell_retinopathy

    Normal adult hemoglobin A molecule comprises two α and two β globin chains associated with a heme ring. Mutation at the 6th position of the beta chain is the cause of sickle cell disease. [ 10 ] Due to sickle cell disease, vascular occlusion may occur in the conjunctiva, iris, retina, or choroid.

  9. Gottron's sign - Wikipedia

    en.wikipedia.org/wiki/Gottron's_sign

    Gottron's sign is a pathognomonic cutaneous manifestation associated with dermatomyositis (DM), which is an inflammatory disorder affecting the skin and muscles. [1] The primary lesion of dermatomyositis appears as a violaceous, macular erythema with a symmetric distribution, which may progress and become poikilodermatous (atrophic with telangiectasia and pigmentary changes) and indurated (as ...