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purpura trombotická trombocytopenická

  1. Subject h.purpura trombotická trombocytopenická
    Subject h.Purpura, Thrombotic Thrombocytopenic
    Entry termspurpura trombotická trombopenická
    purpura trombotická trombocytopenická vrodená
    purpura trombotická trombocytopenická kongenitálna
    purpura trombotická trombocytopenická familiárna
    anémia mikroangiopatická hemolytická vrodená
    anémia mikroangiopatická hemolytická kongenitálna
    mikroangiopatia trombotická familiárna
    Moskowitzova choroba
    Moschkowitzova choroba
    Schulman-Upshawov syndróm
    Upshawov-Schulmanov syndróm
    Upshaw-Schulmanov syndróm
    deficiencia Upshawovho faktora
    deficit Upshawovho faktora
    English X referencesMoschkowitz Disease
    Purpura, Thrombotic Thrombopenic
    Thrombotic Thrombocytopenic Purpura, Congenital
    Thrombotic Thrombocytopenic Purpura, Familial
    Scope note in EnglishAn acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases.
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    (2) - CiBaMed
    (2) - BOOKS
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Number of the records: 1  

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