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Humoral immune response to ADAMTS13 in acquired thrombotic thrombocytopenic purpura

✍ Scribed by W. POS; B. M. LUKEN; N. SORVILLO; J. A. KREMER HOVINGA; J. VOORBERG

Book ID
109154757
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
392 KB
Volume
9
Category
Article
ISSN
1538-7933

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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