- vitelliform degeneration
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вителиформная, желтоподобная дегенерация
Англо-русский офтальмологический словарь. 2010.
Англо-русский офтальмологический словарь. 2010.
vitelliform degeneration — degeneration of the macula of the eye that is inherited as a dominant characteristic and usually starts in childhood. There is widespread abnormality of retinal pigment epithelium (see retina) with the accumulation of a yellowish material,… … Medical dictionary
vitelliform degeneration — Best s disease degeneration of the macula of the eye that is inherited as a dominant characteristic and usually starts in childhood. There is widespread abnormality of retinal pigment epithelium (see retina) with the accumulation of a yellowish… … The new mediacal dictionary
degeneration — 1. Deterioration; passing from a higher to a lower level or type. 2. A worsening of mental, physical, or moral qualities. 3. A retrogressive pathologic change in cells or tissues, in consequence of which their functions are often impaired or… … Medical dictionary
vitelliform macular degeneration — vitelline macular degeneration Best disease … Medical dictionary
Macular degeneration — Classification and external resources Picture of the fundus showing intermediate age related macular degeneration. ICD 10 … Wikipedia
Best's disease — vitelliform degeneration … The new mediacal dictionary
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary
degeneración viteliforme de Best — Eng. Vitelliform degeneration of Best Ver degeneración macular congénita … Diccionario de oftalmología
Best's disease — see vitelliform degeneration F. Best (20th century), German physician … Medical dictionary
Bestrophin 1 — Bestrophin 1, also known as BEST1, is a human gene.cite web | title = Entrez Gene: BEST1 bestrophin 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=7439| accessdate = ] PBB Summary section title = summary … Wikipedia
Peripherin 2 — (retinal degeneration, slow), also known as PRPH2, is a human gene.cite web | title = Entrez Gene: PRPH2 peripherin 2 (retinal degeneration, slow)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5961|… … Wikipedia