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  2. Choroideremia - Wikipedia

    en.wikipedia.org/wiki/Choroideremia

    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.

  3. Scleral reinforcement surgery - Wikipedia

    en.wikipedia.org/wiki/Scleral_reinforcement_surgery

    The surgery aims to cover the thinning posterior pole with a supportive material to withstand intraocular pressure and prevent further progression of the posterior staphyloma. The strain is reduced, although damage from the pathological process cannot be reversed. By stopping the progression of the disease, vision may be maintained or improved.

  4. Lattice degeneration - Wikipedia

    en.wikipedia.org/wiki/Lattice_degeneration

    Lattice degeneration is a disease of the human eye wherein the peripheral retina becomes atrophic in a lattice pattern. Usually, this happens slowly over time and does not cause any symptoms, and medical intervention is neither needed nor recommended.

  5. Macular degeneration - Wikipedia

    en.wikipedia.org/wiki/Macular_degeneration

    Sorsby's fundus dystrophy is an autosomal dominant, retinal disease characterized by sudden acuity loss resulting from untreatable submacular neovascularisation Stargardt's disease (juvenile macular degeneration, STGD) is an autosomal recessive retinal disorder characterized by juvenile-onset macular dystrophy, alterations of the peripheral ...

  6. Retinal tuft - Wikipedia

    en.wikipedia.org/wiki/Retinal_tuft

    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. [5]

  7. Retinal vasculopathy with cerebral leukoencephalopathy and ...

    en.wikipedia.org/wiki/Retinal_vasculopathy_with...

    Retinal vasculopathy with cerebral leukocencephalopathy and systemic manifestations (RVCL or RVCL-S, also previously known as retinal vasculopathy with cerebral leukodystrophy, RVCL; or cerebroretinal vasculopathy, CRV; or hereditary vascular retinopathy, HVR; or hereditary endotheliopathy, retinopathy, nephropathy, and stroke, HERNS) is an inherited condition resulting from a frameshift ...

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