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DeCS
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Descriptor English:
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Purpura, Thrombotic Thrombocytopenic
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Descriptor Spanish:
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Púrpura Trombocitopénica Trombótica
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Descriptor Portuguese:
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Púrpura Trombocitopênica Trombótica
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Synonyms English:
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Congenital Thrombotic Thrombocytopenic Purpura
Familial Thrombotic Thrombocytopenia Purpura
Familial Thrombotic Thrombocytopenic Purpura
Microangiopathic Hemolytic Anemia, Congenital
Moschcowitz Disease
Schulman-Upshaw Syndrome
Thrombotic Microangiopathy, Familial
Thrombotic Thrombocytopenic Purpura
Upshaw Factor, Deficiency of
Upshaw-Schulman Syndrome
Disease, Moschcowitz
Disease, Moschkowitz
Familial Thrombotic Microangiopathy
Microangiopathy, Familial Thrombotic
Schulman Upshaw Syndrome
Syndrome, Schulman-Upshaw
Syndrome, Upshaw-Schulman
Thrombocytopenic Purpura, Thrombotic
Thrombopenic Purpura, Thrombotic
Thrombotic Thrombopenic Purpura
Upshaw Schulman Syndrome
Purpura, Thrombotic Thrombopenic
Moschkowitz Disease
Thrombotic Thrombocytopenic Purpura, Congenital
Thrombotic Thrombocytopenic Purpura, Familial
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Tree Number:
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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
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Definition English:
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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. |
History Note English:
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1986; use PURPURA, THROMBOTIC THROMBOPENIC 1965-1985
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Allowable Qualifiers English:
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Record Number:
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12133
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Unique Identifier:
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D011697
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Occurrence in VHL:
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Similar:
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DeCS CID-10 SciELO LILACS LIS
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