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  2. Thrombotic thrombocytopenic purpura - Wikipedia

    https://en.wikipedia.org/wiki/Thrombotic...

    Thrombotic thrombocytopenic purpura (TTP) is a blood disorder that results in blood clots forming in small blood vessels throughout the body. [2] This results in a low platelet count , low red blood cells due to their breakdown , and often kidney , heart , and brain dysfunction. [ 1 ]

  3. Thrombocytopenic purpura - Wikipedia

    https://en.wikipedia.org/wiki/Thrombocytopenic_purpura

    Thrombocytopenic purpura are purpura associated with a reduction in circulating blood platelets which can result from a variety of causes, [1] such as kaposi sarcoma. Types [ edit ]

  4. Hemolytic–uremic syndrome - Wikipedia

    https://en.wikipedia.org/wiki/Hemolytic–uremic_syndrome

    The TTP leads to platelet trapping (and thrombocytopenia), red blood cell destruction (and anemia), and end organ damage that is characteristically seen with HUS and TTP. [34] HUS is one of the thrombotic microangiopathies, a category of disorders that includes STEC-HUS, aHUS, and thrombotic thrombocytopenic purpura (TTP).

  5. Thrombocytopenia - Wikipedia

    https://en.wikipedia.org/wiki/Thrombocytopenia

    Adults may have large, blood-filled bullae in the mouth. [10] If the person's platelet count is between 30,000 and 50,000/μL, bruising with minor trauma may be expected; if it is between 15,000 and 30,000/μL, spontaneous bruising will be seen (mostly on the arms and legs).

  6. Immune thrombocytopenic purpura - Wikipedia

    https://en.wikipedia.org/wiki/Immune_thrombocytopenic...

    ITP is usually chronic in adults [60] and the probability of durable remission is 20–40 percent. [19] The male to female ratio in the adult group varies from 1:1.2 to 1.7 in most age ranges (childhood cases are roughly equal for both sexes) and the median age of adults at the diagnosis is 56–60. [12]

  7. Inherited thrombotic thrombocytopenic purpura - Wikipedia

    https://en.wikipedia.org/wiki/Inherited_thrombotic...

    Thrombotic thrombocytopenic purpura (TTP) is a life-threatening disorder characterized by thrombocytopenia and microangiopathic hemolytic anemia accompanied by variable neurological dysfunction, kidney failure, and fever. It is caused by severely reduced activity of the von Willebrand factor-cleaving protease ADAMTS13.

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  9. Upshaw–Schulman syndrome - Wikipedia

    https://en.wikipedia.org/wiki/Upshaw–Schulman_syndrome

    Upshaw–Schulman syndrome (USS) is the recessively inherited form of thrombotic thrombocytopenic purpura (TTP), a rare and complex blood coagulation disease. USS is caused by the absence of the ADAMTS13 protease resulting in the persistence of ultra large von Willebrand factor multimers (ULvWF), causing episodes of acute thrombotic microangiopathy with disseminated multiple small vessel ...

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