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Other names: 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
378.8 Other disorders of binocular eye movements; 378.9 Unspecified; 379 Other disorders of eye. 379.0 Scleritis and episcleritis; 379.1 Other disorders of sclera; 379.2 Disorders of vitreous body; 379.3 Aphakia and other disorders of lens; 379.4 Anomalies of pupillary function; 379.5 Nystagmus and other irregular eye movements; 379.8 Other ...
This is a partial list of human eye diseases and disorders. The World Health Organization (WHO) publishes a classification of known diseases and injuries, the International Statistical Classification of Diseases and Related Health Problems, or ICD-10. This list uses that classification.
Schwartz hypothesized iridocyclitis as the cause of elevated intraocular pressure, but Davidorf suggested that the elevated IOP may be due to obstruction of trabecular meshwork by pigmented cells representing photoreceptor outer segments from retinal pigment epithelium that migrate anteriorly within the aqueous humor. [1]
Pachychoroid disorders of the macula represent a group of diseases affecting the central part of the retina of the eye, the macula. Due to thickening and congestion of the highly vascularized layer underneath the macula, the choroid, damage to the retinal pigment epithelium and the retinal photoreceptor cells ensues. This leads to impaired vision.
However, the retinal pigment epithelium (RPE) rapidly becomes involved, leading to a retinal dystrophy primarily involving the macula. The histological examination of the eyes of one such patient showed that the outer nuclear layer of cones and rods had disappeared completely, whereas the RPE showed pronounced pigment changes.
Ocular albinism type 1 (OA1) is the most common type of ocular albinism, with a prevalence rate of 1:50,000. [1] [2] It is an inheritable classical Mendelian type X-linked recessive disorder wherein the retinal pigment epithelium lacks pigment while hair and skin appear normal.
Symptoms include blurred vision in both eyes, but the onset may occur at a different time in each eye. There are yellow-white placoid lesions in the posterior pole at the level of the retinal pigment epithelium. Some suggest a genetic predisposition to the disease, while others postulate an abnormal immune response to a virus. [2]