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Deficiency of ADAMTS13 in thrombotic thrombocytopenic purpura

✍ Scribed by Han-Mou Tsai


Publisher
Carden Jennings Publishing
Year
2002
Tongue
English
Weight
991 KB
Volume
76
Category
Article
ISSN
0925-5710

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ADAMTS13 mutations and polymorphisms in
✍ Luca A. Lotta; Isabella Garagiola; Roberta Palla; Andrea Cairo; Flora Peyvandi πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 223 KB

Congenital thrombotic thrombocytopenic purpura (TTP) (also known as Upshaw-Schulman syndrome, USS) is a rare, life-threatening disease characterized by thrombocytopenia and microangiopathic hemolytic anemia, associated with the deficiency of the von Willebrand factor-cleaving protease (ADAMTS13) due

Thrombotic thrombocytopenic purpura with
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## Abstract Arterial thrombotic events, thrombocytopenia, and hemolytic anemia with schistocytes may be encountered in the setting of both thrombotic thrombocytopenic purpura (TTP) and primary antiphospholipid syndrome (APS). We report 2 cases of TTP occurring in patients with definite primary APS.