Ehlers–Danlos syndrome — Classification and external resources The collagen fibril and EDS. (a) Normal collagen fibrils are of uniform size and spacing. Fibrils from a patient with dermatosparaxis (b) show dramatic alterations in fibril morphology with severe effects on… … Wikipedia
Ehlers-Danlos syndrome — Ehlers Danlos syndrome. См. синдром Элерса Данло. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
Ehlers-Danlos syndrome — Infobox Disease | Name = Ehlers Danlos syndrome | ICD10 = ICD10|Q|79|6|q|65 | ICD9 = ICD9|756.83 | OMIM = | MedlinePlus = 001468 eMedicineSubj = derm eMedicineTopic = 696 eMedicine mult = eMedicine2|ped|654 | MeshID = D004535 Ehlers Danlos… … Wikipedia
Ehlers-Danlos syndrome — A heritable disorder of connective tissue with easy bruising, joint hypermobility (loose joints), skin laxity, and weakness of tissues. There are a number of different types of Ehlers Danlos syndrome (EDS) which share the foregoing features but… … Medical dictionary
ehlers-danlos syndrome — ˈālərzˈdan(ˌ)läs noun Usage: usually capitalized E&D Etymology: after E. Ehlers died 1937 Dan. dermatologist and H.A. Danlos died 1912 French dermatologist : an inherited disorder of connective tissue with several clinical forms characterized… … Useful english dictionary
Ehlers-Danlos syndrome — /ay leuhrz dan los, leuhs/, Pathol. a rare hereditary disease of connective tissue, characterized by joint hypermotility and abnormally stretchable skin. [after Edvard Ehlers (1863 1937), Danish dermatologist, and Henri Alexandre Danlos (1844… … Universalium
Ehlers-Danlos syndrome — any one of a rare group of inherited (autosomal dominant or autosomal recessive) disorders of the connective tissue involving abnormal or deficient collagen, the protein that gives the body tissues strength. There are several types of differing… … The new mediacal dictionary
Ehlers-Danlos syndrome — See dermatosparaxis … Dictionary of molecular biology
Syndrome d'Ehlers-Danlos type vasculaire — Pour les articles homonymes, voir Syndrome d Ehlers Danlos. Le syndrome d Ehlers Danlos type vasculaire est, dans le groupe des syndromes d Ehlers Danlos, caractérisé par une peau fine, translucide, se lésant facilement; une apparence du visage… … Wikipédia en Français
Ehlers-Danlos-Syndrom — Klassifikation nach ICD 10 Q79.6 Ehlers Danlos Syndrom … Deutsch Wikipedia
Danlos syndrome — Better known today as Ehlers Danlos syndrome (EDS), this is an inherited disorder with easy bruising, joint hypermobility (loose joints), skin laxity, and weakness of tissues. There are a number of different Ehlers Danlos syndromes which share… … Medical dictionary
