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1 помутнение роговицы
1) General subject: corneal clouding2) Medicine: aglia, wall eye, corneal haze, corneal opacityУниверсальный русско-английский словарь > помутнение роговицы
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2 помутнение роговой оболочки глаза
Medicine: nebula, corneal cloudingУниверсальный русско-английский словарь > помутнение роговой оболочки глаза
См. также в других словарях:
Corneal dystrophy — is a group of disorders, characterised by a noninflammatory, inherited, bilateral opacity of the transparent front part of the eye called the cornea. The distrophies could be subdivided based on specie affected: Corneal dystrophies in human… … Wikipedia
opacidad corneal y mancha rojo-cereza — Eng. Corneal clouding and cherry red spot Ver síndrome de Golderg Cotlier … Diccionario de oftalmología
Congenital stromal corneal dystrophy — Classification and external resources The cornea is particularly opaque in the anterior stroma by slit lamp biomicroscopy OMIM … Wikipedia
Mucopolysaccharidosis — MPS I redirects here. For zhuyin or bopomofo, a phonetic system for romanizing Chinese, also known as Mandarin Phonetic Symbols I, see Bopomofo. Mucopolysaccharidosis Classification and external resources ICD 10 E76 ICD 9 … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
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
Morquio syndrome — Classification and external resources ICD 10 E76.2 ICD 9 277.5 … Wikipedia
Hurler syndrome — An inherited error of metabolism in which there is deficiency of the enzyme alpha L iduronidase which normally breaks down molecules called mucopolysaccharides. Without the activity of this enzyme, there is an abnormal accumulation of… … Medical dictionary
Morquio syndrome — An inherited error in carbohydrate metabolism that results in mucopolysaccharide accumulation and severe skeletal defects. The defects are present at birth and include severe deformity of the spine and chest, short neck, loose and enlarged joints … Medical dictionary
Sialolipidose — Klassifikation nach ICD 10 E75.1 Sonstige Gangliosidosen Mukolipidose IV … Deutsch Wikipedia
Mucolipidosis type IV — Classification and external resources ICD 10 E75.1 OMIM 252650 DiseasesDB … Wikipedia
