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Retinoschisis is an eye disease characterized by the abnormal splitting of the retina's neurosensory layers, usually in the outer plexiform layer.Retinoschisis can be divided into degenerative forms which are very common and almost exclusively involve the peripheral retina and hereditary forms which are rare and involve the central retina and sometimes the peripheral retina.
Retinal detachment occurs when the retina separates from the layers underneath it. [2] This impairs its function, potentially leading to vision loss. [2] [4] Retinal detachment often requires urgent medical intervention to prevent permanent vision loss. [3] Retinal detachments are divided into three main types based on their distinct causes. [6]
Uveitis with poliosis of the eyelashes. The disease is characterised by bilateral diffuse uveitis, with pain, redness and blurring of vision.The eye symptoms may be accompanied by a varying constellation of systemic symptoms, such as auditory (tinnitus, [6] vertigo, [6] and hypoacusis), neurological (meningismus, with malaise, fever, headache, nausea, abdominal pain, stiffness of the neck and ...
Ischemic optic neuropathies are classified based on the location of the damage and the cause of reduced blood flow if known. [3] Anterior ischemic optic neuropathy (AION) includes diseases that affect the optic nerve head and cause swelling of the optic disc. These diseases often cause sudden rapid visual loss in one eye.
Metamorphopsia is a symptom of several common retinal and macular diseases, therefore treating the underlying disorder can improve symptoms. For people who have conditions such as epiretinal membrane (ERM), macular holes and retinal detachment, decreased metamorphopsia is associated with an increase in visual acuity. [4]
People with the condition usually display redness of the eye, white or off-white colored patches that are patches of retinal necrosis. [3] ARN can progress into other conditions such as uveitis, detachment of the retina, and ultimately can lead to blindness. [4] The disease was first characterized in 1971, in Japan.
Eales disease is a type of obliterative vasculopathy, also known as angiopathia retinae juvenilis, periphlebitis retinae or primary perivasculitis of the retina.It was first described by the British ophthalmologist Henry Eales (1852–1913) in 1880 [1] and is a rare ocular disease characterized by inflammation and possible blockage of retinal blood vessels, abnormal growth of new blood vessels ...
Surgically correct retinal detachment by scleral buckle or pars plana vitrectomy. [1] Prior to surgery, oral or topical anti glaucoma drugs may be used to reduce IOP. [1] After surgical correction of the retinal detachment, the condition resolves, aqueous cells disappear and IOP normalizes. [3] The condition is not responsive to corticosteroid ...