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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Purpura, Thrombotic Thrombocytopenic | Legal notice |
Other terms
Purpuras, Thrombotic Thrombocytopenic,Thrombocytopenic Purpura, Thrombotic,Thrombocytopenic Purpuras, Thrombotic,Thrombotic Thrombocytopenic Purpura,Thrombotic Thrombocytopenic Purpuras,Moschkowitz Disease,Disease, Moschkowitz,Purpura, Thrombotic Thrombopenic,Purpuras, Thrombotic Thrombopenic,Thrombopenic Purpura, Thrombotic,Thrombopenic Purpuras, Thrombotic,Thrombotic Thrombopenic Purpura,Thrombotic Thrombopenic Purpuras,Moschcowitz Disease,Disease, Moschcowitz,Familial Thrombotic Thrombocytopenic Purpura,Thrombotic Thrombocytopenic Purpura, Familial,Congenital Thrombotic Thrombocytopenic Purpura,Thrombotic Thrombocytopenic Purpura, Congenital,Schulman-Upshaw Syndrome,Schulman Upshaw Syndrome,Syndrome, Schulman-Upshaw
Description
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.
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Legal notice
The U.S. National Library of Medicine is the creator, maintainer, and provider of the data above.
The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
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