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  2. Chronic progressive external ophthalmoplegia - Wikipedia

    en.wikipedia.org/wiki/Chronic_progressive...

    Ophthalmology. Chronic progressive external ophthalmoplegia ( CPEO) is a type of eye disorder characterized by slowly progressive inability to move the eyes and eyebrows. [ 1] It is often the only feature of mitochondrial disease, in which case the term CPEO may be given as the diagnosis. In other people suffering from mitochondrial disease ...

  3. Corneal ectatic disorders - Wikipedia

    en.wikipedia.org/wiki/Corneal_ectatic_disorders

    Keratoconus, a progressive, noninflammatory, bilateral, asymmetric disease, characterized by paraxial stromal thinning and weakening that leads to corneal surface distortion. [2] Keratoglobus, a rare noninflammatory corneal thinning disorder, characterised by generalised thinning and globular protrusion of the cornea. [3]

  4. Glaucoma - Wikipedia

    en.wikipedia.org/wiki/Glaucoma

    Glaucoma is a group of eye diseases that lead to damage of the optic nerve, which transmits visual information from the eye to the brain. Glaucoma may cause vision loss if left untreated. It has been called the "silent thief of sight" because the loss of vision usually occurs slowly over a long period of time. [ 5]

  5. Retinitis pigmentosa - Wikipedia

    en.wikipedia.org/wiki/Retinitis_pigmentosa

    1 in 4,000 people [ 1] Retinitis pigmentosa ( RP) is a genetic disorder of the eyes that causes loss of vision. [ 1] Symptoms include trouble seeing at night and decreasing peripheral vision (side and upper or lower visual field). [ 1] As peripheral vision worsens, people may experience "tunnel vision". [ 1]

  6. Central serous chorioretinopathy - Wikipedia

    en.wikipedia.org/wiki/Central_serous_chorio...

    Central serous chorioretinopathy ( CSC or CSCR ), also known as central serous retinopathy ( CSR ), is an eye disease that causes visual impairment, often temporary, usually in one eye. [ 1][ 2] When the disorder is active it is characterized by leakage of fluid under the retina that has a propensity to accumulate under the central macula.

  7. Stargardt disease - Wikipedia

    en.wikipedia.org/wiki/Stargardt_disease

    Genetic. Diagnostic method. Slit lamp. Treatment. None. 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).

  8. Geographic atrophy - Wikipedia

    en.wikipedia.org/wiki/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 visual function ...

  9. Iridocorneal endothelial syndrome - Wikipedia

    en.wikipedia.org/wiki/Iridocorneal_endothelial...

    Iridocorneal endothelial (ICE) syndromes are a spectrum of diseases characterized by slowly progressive abnormalities of the corneal endothelium and features including corneal edema, iris distortion, and secondary angle-closure glaucoma. [ 1][ 2][ 3] ICE syndromes are predominantly unilateral and nonhereditary. [ 1][ 2][ 3] The condition occurs ...

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