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1 предполагаемый возбудитель болезни Крейтцфельдта—Якоба
Medicine: Creutzfeldt-Jakob agent (то-то считает, что это «медленный вирус», кто-то — прион)Универсальный русско-английский словарь > предполагаемый возбудитель болезни Крейтцфельдта—Якоба
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2 F02.1
рус Деменция при болезни Крейтцфельдта-Якобаeng Dementia in Creutzfeldt-Jakob disease ( A81.0+). A progressive dementia with extensive neurological signs, due to specific neuropathological changes that are presumed to be caused by a transmissible agent. Onset is usually in middle or later life, but may be at any adult age. The course is subacute, leading to death within one to two years.
См. также в других словарях:
Creutzfeldt–Jakob disease — Classification and external resources Tonsil biopsy in variant CJD. Prion Protein immunostaining. ICD 10 A … Wikipedia
Creutzfeldt-Jakob disease — Infobox Disease Name = Creutzfeldt Jakob disease Caption = DiseasesDB = 3166 ICD10 = ICD10|A|81|0|a|80, ICD10|F|02|1|f|00 ICD9 = ICD9|046.1 ICDO = OMIM = 123400 MedlinePlus = eMedicineSubj = neuro eMedicineTopic = 725 MeshID = D007562 Creutzfeldt … Wikipedia
Creutzfeldt-Jakob disease — /kroyts felt yah kawp/, Pathol. a rare, usually fatal brain disorder caused by an unidentified pathogen and characterized by progressive dementia, blindness, and involuntary movements. Also, Creutzfeldt Jacob disease. Also called Jakob… … Universalium
Creutzfeldt-Jakob disease — Creutz·feldt Ja·kob disease also Creutz·feld Ja·kob disease .krȯits .felt .yä (.)kōb n a rare progressive fatal spongiform encephalopathy now usu. considered to be caused by a prion and marked by the development of porous brain tissue, premature … Medical dictionary
Creutzfeldt-Jakob — Maladie de Creutzfeldt Jakob Maladie de Creutzfeldt Jakob CIM 10 : A81.0, F02.1 La maladie de Creutzfeldt Jakob (MCJ) est une dégénérescence du système nerveux central caractérisée par l accumulation d un prion (forme anormale d une protéine qui… … Wikipédia en Français
Creutzfeldt Jakob — Maladie de Creutzfeldt Jakob Maladie de Creutzfeldt Jakob CIM 10 : A81.0, F02.1 La maladie de Creutzfeldt Jakob (MCJ) est une dégénérescence du système nerveux central caractérisée par l accumulation d un prion (forme anormale d une protéine qui… … Wikipédia en Français
Creutzfeldt-Jakob disease — CJD a rapidly progressive rare neurological disease, a form of human spongiform encephalopathy in which dementia progresses to death after a period of 3–12 months. There is no effective treatment. The causative agent is an abnormal prion protein… … The new mediacal dictionary
Creutzfeldt-Jakob disease new variant — (nvCJD) a variant of Creutzfeldt Jakob disease occurring almost exclusively in the United Kingdom, having a younger age of onset than is seen in Creutzfeldt Jakob disease, and caused by the same agent that causes bovine spongiform encephalopathy … Medical dictionary
Maladie de Creutzfeldt-Jakob — Classification et ressources externes Accumulation d un prion. CIM 10 … Wikipédia en Français
Variant Creutzfeldt-Jakob disease — Abbreviated vCJD. A human disease thought due to the same infectious agent as bovine spongiform encephalopathy (BSE), or mad cow disease. Both the human and bovine disorders are invariably fatal brain diseases with unusually long incubation… … Medical dictionary
New variant Creutzfeldt-Jakob disease — Abbreviated nvCJD. A human disease thought due to the same infectious agent as bovine spongiform encephalopathy (BSE), or mad cow disease. Both the human and bovine disorders are invariably fatal brain diseases with unusually long incubation… … Medical dictionary
