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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/3252
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dc.contributor.authorDumbrava, Vlada
dc.contributor.authorOnu, Vera
dc.contributor.authorCasapciuc, Marina
dc.contributor.authorChirvas, Elena
dc.contributor.authorMunteanu, Diana
dc.contributor.authorDreglea, Victoria
dc.date.accessioned2019-06-25T02:50:22Z-
dc.date.available2019-06-25T02:50:22Z-
dc.date.issued2008
dc.identifier.citationDUMBRAVA, Vlada, ONU, Vera. et al. Un caz clinic de sindrom Lyell. In: Anale Științifice ale USMF “Nicolae Testemiţanu”. Ed. a 9-a. Chișinău: CEP Medicina, 2008, vol. 3: Probleme actuale în medicina internă, pp. 160-166.en_US
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/3252-
dc.descriptionCatedra medicina internă №r 4 USMF ״N.Testemiţanu״ Spitalul Clinic Republicanen_US
dc.description.abstractLyell syndrome (acute toxic epidermal necrose) is an acute, vital dangerous disturbance, which is characterized by diffuse adulteration of the teguments and mucosa with bull formation, epidermal necrolisis, skin exfoliation associated with severe intoxication and function lesion of all organs and systems. This syndrome is included in the rare and little – known disease group. Sindromul Lyell (necroza epidermală toxică acută, necroepidermoliza buloasă, toxidermia buloasă, sindromul cutanatului “ars”) este o maladie acută, vital periculoasă, ce se caracterizează prin alterarea difuză a tegumentelor şi mucoaselor cu formarea bulelor, necroliza epidermală, exfolierea pielii, asociată cu intoxicaţie gravă şi alterarea funcţiilor tuturor organelor şi sistemelor. Acest sindrom este inclus în grupul maladiilor rare şi puţin cunoscute.en_US
dc.language.isoroen_US
dc.publisherCEP "Medicina"en_US
dc.titleUn caz clinic de sindrom Lyellen_US
dc.title.alternativeClinical case of Lyell syndromeen_US
dc.typeArticleen_US
Appears in Collections:Gastroenterologie, alergologie

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