Purpura, Thrombotic Thrombocytopenic


Congenital Thrombotic Thrombocytopenic Purpura

Disease, Moschcowitz

Disease, Moschkowitz

Familial Thrombotic Microangiopathy

Familial Thrombotic Thrombocytopenia Purpura

Familial Thrombotic Thrombocytopenic Purpura

Microangiopathic Hemolytic Anemia, Congenital

Microangiopathy, Familial Thrombotic

Moschcowitz Disease

Moschkowitz Disease

Purpura, Thrombotic Thrombopenic

Schulman Upshaw Syndrome

Schulman-Upshaw Syndrome

Syndrome, Schulman-Upshaw

Syndrome, Upshaw-Schulman

Thrombocytopenic Purpura, Thrombotic

Thrombopenic Purpura, Thrombotic

Thrombotic Microangiopathy, Familial

Thrombotic Thrombocytopenic Purpura

Thrombotic Thrombocytopenic Purpura, Congenital

Thrombotic Thrombocytopenic Purpura, Familial

Thrombotic Thrombopenic Purpura

Upshaw Factor, Deficiency of

Upshaw Schulman Syndrome

Upshaw-Schulman Syndrome

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.