- retina atrophy
- Netzhautatrophie f
Fachwörterbuch Medizin Englisch-Deutsch. 2013.
retina atrophy
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Atrophy — Wasting away or diminution. Muscle atrophy is wasting of muscle, decrease in muscle mass. A nerve can also show atrophy. For example, atrophy of the optic nerve diminishes vision. * * * A wasting of tissues, organs, or the entire body, as from… … Medical dictionary
Retina — For the Retina display in the iPhone 4, see iPhone 4#Display. Retina Right human eye cross sectional view. Courtesy NIH National Eye Institute. Many animals hav … Wikipedia
Progressive retinal atrophy — (PRA) is a group of genetic diseases seen in certain breeds of dogs and, more rarely, cats. It is characterized by the bilateral degeneration of the retina, causing progressive vision loss culminating in blindness. The condition in nearly all… … Wikipedia
optic atrophy — ▪ pathology degeneration of the optic nerve (the second cranial nerve) due to direct or indirect damage to a particular type of retinal (retina) cell, called ganglion cells, whose axonal (axon) projections collectively make up the optic… … Universalium
gyrate atrophy — n progressive degeneration of the choroid and pigment epithelium of the retina that is inherited as an autosomal recessive trait and is characterized esp. by myopia, constriction of the visual field, night blindness, and cataracts * * * a… … Medical dictionary
Yellow atrophy — Yellow Yel low (y[e^]l l[ o]), a. [Compar. {Yellower} (y[e^]l l[ o]*[ e]r); superl. {Yellowest}.] [OE. yelow, yelwe, [yogh]elow, [yogh]eoluw, from AS. geolu; akin to D. geel, OS. & OHG. gelo, G. gelb, Icel. gulr, Sw. gul, Dan. guul, L. helvus… … The Collaborative International Dictionary of English
gyrate atrophy — a hereditary condition causing night blindness and constricted visual fields, usually developing in the third decade of life. Clinically it is characterized by a progressive atrophy of the choroid and retina … The new mediacal dictionary
gyrate atrophy of choroid and retina — an autosomal recessive form of tapetoretinal degeneration, caused by mutations in the OAT gene (locus: 10q26) that result in ornithine aminotransferase deficiency and hyperornithinemia. It is marked by ring shaped areas of thinning in the… … Medical dictionary
atrophia choroideae et retinae — atrophy of the choroid and retina, formerly associated with night blindness … Medical dictionary
eye disease — Introduction any of the diseases or disorders that affect the human eye (eye, human). This article briefly describes the more common diseases of the eye and its associated structures, the methods used in examination and diagnosis, and the… … Universalium
nervous system disease — Introduction any of the diseases or disorders that affect the functioning of the human nervous system (nervous system, human). Everything that humans sense, consider, and effect and all the unlearned reflexes of the body depend on the… … Universalium
