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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.
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.
The risk of retinal detachment is the greatest in the first 6 weeks following a vitreous detachment, but can occur over 3 months after the event.. The risk of retinal tears and detachment associated with vitreous detachment is higher in patients with myopic retinal degeneration, lattice degeneration, and a familial or personal history of previous retinal tears/detachment.
(H35.3) Age-related macular degeneration — the photosensitive cells in the macula malfunction and over time cease to work (H35.3) Macular degeneration — loss of central vision, due to macular degeneration Bull's Eye Maculopathy (H35.3) Epiretinal membrane — a transparent layer forms and tightens over the retina (H35.4) Peripheral retinal ...
Retinal detachment is typically painless, with symptoms often starting in the peripheral vision. [3] [9] [10] Symptoms of retinal detachment, as well as posterior vitreous detachment (which often, but not always, precedes it), may include: [3] [4] [9] [10] [12] Floaters suddenly appearing in the field of vision or a sudden increase in the ...
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 ...
A vitreo-retinal specialist (an ophthalmologist specialized in treatment of retinal diseases) should be consulted for proper management of the case. [ citation needed ] Presumed ocular histoplasmosis syndrome and age-related macular degeneration (AMD) have been successfully treated with laser, anti-vascular endothelial growth factors and ...
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).