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1 Stargardt's disease
( Ophth) Stargardtsche Krankheit f, Stargardtsches Syndrom n, juvenile Makuladegeneration f, Makuladegeneration f mit OptikusatrophieFachwörterbuch Medizin Englisch-Deutsch > Stargardt's disease
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2 Stargardt's macular degeneration
Fachwörterbuch Medizin Englisch-Deutsch > Stargardt's macular degeneration
См. также в других словарях:
Stargardt disease (macular degeneration) — Star·gardt disease (macular degeneration) (shtahrґgahrt) [Karl Bruno Stargardt, German ophthalmologist, 1875–1927] see under disease … Medical dictionary
Macular degeneration — Classification and external resources Picture of the fundus showing intermediate age related macular degeneration. ICD 10 … Wikipedia
Macular degeneration — A disease that progressively destroys the macula, the central portion of the retina, impairing central vision. Macular degeneration rarely causes blindness because only the center of vision is affected. However, injury to the macula in the center … Medical dictionary
Stargardt macular degeneration — see under disease … Medical dictionary
Stargardt disease — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 31282 ICD10 = ICD9 = ICDO = OMIM = 248200 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Stargardt disease, or fundus flavimaculatus, has been vastly reported as an autosomal… … Wikipedia
Stargardt disease — An hereditary eye disease that is one of the most frequent causes of macular degeneration in childhood. (The macula is the part of the retina that is responsible for central vision.) The disease has its onset between the ages of 7 and 12 years,… … Medical 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
ABCA4 — ATP binding cassette, sub family A (ABC1), member 4, also known as ABCA4, is a human gene.cite web | title = Entrez Gene: ABCA4 ATP binding cassette, sub family A (ABC1), member 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
ELOVL4 — Elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast) like 4, also known as ELOVL4, is a human gene.cite web | title = Entrez Gene: ELOVL4 elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast) like 4| url =… … Wikipedia
Foundation Fighting Blindness — Formation 1971 Type Non Profit Purpose/focus Fund research that will lead to preve … Wikipedia
HMCN1 — Hemicentin 1, also known as HMCN1, is a human gene.cite web | title = Entrez Gene: HMCN1 hemicentin 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=83872| accessdate = ] PBB Summary section title =… … Wikipedia