- cone dystrophy
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дистрофия колбочек
Англо-русский офтальмологический словарь. 2010.
cone dystrophy
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Cone dystrophy — Classification and external resources Fundus of a 34 year old patient with cone rod dystrophy due to Spinocerebellar Ataxia Type 7 (SCA7). Note that the macular area, and also the mid periphery, are atrophic … Wikipedia
Cone — This disambiguation page lists articles associated with the same title. If an internal link led you here, you may wish to change the link to point directly to the intended article … Wikipedia
Cone cell — Neuron: Cone Cell Normalized responsivity spectra of human cone cells, S, M, and L types NeuroLex ID … Wikipedia
Dystrophy, cone — A disease of the cones, the specialized light sensitive cells that act as photoreceptors in the retina of the eye, providing sharp central vision and color vision. The cone dystrophies are a form of genetic macular degeneration characterized by… … Medical dictionary
dystrophy — Progressive changes that may result from defective nutrition of a tissue or organ. SYN: dystrophia. [dys + G. trophe, nourishment] adiposogenital d. a disorder characterized primarily by obesity and hypogonadotrophic hypogonadism … Medical dictionary
Color blindness — Colorblind and Colourblind redirect here. For other uses, see Colorblind (disambiguation). Color blindness or color deficiency Classification and external resources An 1895 illustration of normal vision and various kinds of color blindness … Wikipedia
GUCA1A — Guanylate cyclase activator 1A (retina), also known as GUCA1A, is a human gene.cite web | title = Entrez Gene: GUCA1A guanylate cyclase activator 1A (retina)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
Monochromacy — Classification and external resources Monochromacy (an abnormality) is a disease state in human vision, native (normal) physiology for pinnipeds (such as Neophoca cinerea shown here), cetaceans, Owl Monkeys and other animals Monochromacy, also… … Wikipedia
List of diseases (C) — A list of diseases in the English wikipedia.C* C syndrome * C1 esterase deficiency (angioedema)CaCac Cal* Cacchi Ricci disease * CACH syndrome * Cafe au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… … Wikipedia
Scanning laser ophthalmoscopy — Retinal image of a left eye via Optos Optomap. Scanning laser ophthalmoscopy (SLO) is a method of examination of the eye. It uses the technique of confocal laser scanning microscopy for diagnostic imaging of retina or cornea of the human eye. As… … Wikipedia
RLBP1 — Retinaldehyde binding protein 1, also known as RLBP1, is a human gene.cite web | title = Entrez Gene: RLBP1 retinaldehyde binding protein 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=6017| accessdate … Wikipedia
