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MeSH 搜索器

Purpura, Thrombotic Thrombocytopenic

An 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.
推出的年份: 1986
副标题
树号: C15.378.100.802.687.680, C15.378.140.855.925.750.680, C15.378.925.850, C23.550.414.950.687.680, C23.888.885.687.687.680
MeSH 单一 ID: D011697
进入的组:
  • Thrombocytopenic Purpura, Thrombotic
  • Thrombotic Thrombocytopenic Purpura
  • Purpura, Thrombotic Thrombopenic
  • Thrombopenic Purpura, Thrombotic
  • Thrombotic Thrombopenic Purpura
  • Moschcowitz Disease
  • Moschkowitz Disease
  • Congenital Thrombotic Thrombocytopenic Purpura
  • Schulman-Upshaw Syndrome
  • Schulman Upshaw Syndrome
  • Upshaw-Schulman Syndrome
  • Upshaw Schulman Syndrome
  • Thrombotic Thrombocytopenic Purpura, Congenital
  • Upshaw Factor, Deficiency of
  • Microangiopathic Hemolytic Anemia, Congenital
  • Thrombotic Microangiopathy, Familial
  • Familial Thrombotic Microangiopathy
  • Microangiopathy, Familial Thrombotic
  • Familial Thrombotic Thrombocytopenic Purpura
  • Thrombotic Thrombocytopenic Purpura, Familial
  • Familial Thrombotic Thrombocytopenia Purpura

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