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  2. Photopsia - Wikipedia

    en.wikipedia.org/wiki/Photopsia

    age-related macular degeneration; vertebrobasilar insufficiency; optic neuritis; visual snow syndrome; Vitreous shrinkage or liquefaction, which is the most common cause of photopsia, causes a pull in vitreoretinal attachments, irritating the retina and causing it to discharge electrical impulses.

  3. Cogan syndrome - Wikipedia

    en.wikipedia.org/wiki/Cogan_syndrome

    Cogan syndrome (also Cogan's syndrome) is a rare disorder characterized by recurrent inflammation of the front of the eye (the cornea) and often fever, fatigue, and weight loss, episodes of vertigo (dizziness), tinnitus (ringing in the ears) and hearing loss. It can lead to deafness or blindness if untreated.

  4. Retinitis pigmentosa - Wikipedia

    en.wikipedia.org/wiki/Retinitis_pigmentosa

    The initial retinal degenerative symptoms of retinitis pigmentosa are characterized by decreased night vision and the loss of the mid-peripheral visual field. [4] The rod photoreceptor cells, which are responsible for low-light vision and are orientated mainly in the retinal periphery, are the retinal processes affected first during non ...

  5. Macular telangiectasia - Wikipedia

    en.wikipedia.org/wiki/Macular_Telangiectasia

    Macular telangiectasia type 2 is commonly under-diagnosed. The findings may appear very similar to diabetic retinopathy, and many cases have been incorrectly ascribed to diabetic retinopathy or age-related macular degeneration. Recognition of this condition can save an affected patient from unnecessarily undergoing extensive medical testing and ...

  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. Stargardt disease - Wikipedia

    en.wikipedia.org/wiki/Stargardt_disease

    Gene therapy is designed to insert a copy of a corrected gene into retinal cells. The hope is to return cell function back to normal and the treatment has the potential to stop disease progression. This therapy will not restore impaired vision back to normal. The research is being undertaken by a partnership between Sanofi and Oxford BioMedica.

  8. Usher syndrome - Wikipedia

    en.wikipedia.org/wiki/Usher_syndrome

    Usher syndrome, also known as Hallgren syndrome, Usher–Hallgren syndrome, retinitis pigmentosa–dysacusis syndrome or dystrophia retinae dysacusis syndrome, [1] is a rare genetic disorder caused by a mutation in any one of at least 11 genes resulting in a combination of hearing loss and visual impairment.

  9. Wagner's disease - Wikipedia

    en.wikipedia.org/wiki/Wagner's_disease

    Wagner's disease is a familial disease of the eye that can cause reduced visual acuity. [1] Wagner's disease was originally described in 1938. This disorder was frequently confused with Stickler syndrome, but lacks the systemic features and high incidence of retinal detachments.

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