Search results
Results from the WOW.Com Content Network
Generally, diseases outlined within the ICD-10 codes H00-H59 within Chapter VII: Diseases of the eye, adnexa should be included in this category. Wikimedia Commons has media related to Diseases and disorders of the eye and adnexa .
CHRPE is a lesion with the retinal pigment epithelial (RPE)— densely packed cells in a single layer forming a blockage between the retina and the choroid— [6] that is generally cordial. There are three variations of CHRPE: solitary, grouped, and atypical, with these being found in ophthalmoscopes. [ 5 ]
Indocyanine green angiography (ICGA), [10] and OCT angiography (OCTA) [11] [12] [13] studies have provided support for choriocapillaris involvement. However, a novel hypothesis was proposed implicating a direct neurotropic infection as a possible underlying cause given the dynamic changes observed along the neuronal pathway of the retina [ 14 ]
Inherited retinal dystrophy/diseases: Back of the eye of a person with mid-stage retinitis pigmentosa. Note pigment deposits in the mid periphery along with retinal atrophy. While the macula is preserved there is some loss of pigmentation around it. Specialty: Ophthalmology, Optometry: Symptoms: Trouble seeing at night, decreased peripheral ...
(H35.4) Peripheral retinal degeneration (H35.5) Hereditary retinal dystrophy (H35.5) Retinitis pigmentosa — genetic disorder; tunnel vision preceded by night-blindness (H35.6) Retinal haemorrhage (H35.7) Separation of retinal layers. Central serous retinopathy; Retinal detachment: Detachment of retinal pigment epithelium
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.
Drusen, from the German word for node or geode (singular, "Druse"), are tiny yellow or white accumulations of extracellular material that build up between Bruch's membrane and the retinal pigment epithelium of the eye. The presence of a few small ("hard") drusen is normal with advancing age, and most people over 40 have some hard drusen. [1]
Cone dystrophy; Fundus of a 45 year-old patient with cone rod dystrophy segregating with a loss-of-function mutation (E1087X) in ABCA4. Note the presence of various-shaped pigment deposits in the posterior pole with atrophy of the retina, while the retina appears less damaged in periphery (upper part of the photograph).