| Literature DB >> 22244722 |
Pier Mannuccio Mannucci1, Massimo Franchini.
Abstract
Thrombotic thrombocytopenic purpura (TTP) is a rare but severe disease characterized by mechanical hemolytic anemia and consumptive thrombocytopenia leading to disseminated microvascular thrombosis that causes signs and symptoms of organ ischemia and functional damage. After the elucidation of the pathophysiology of TTP, thanks to the demonstration of the congenital or acquired (autoimmune) plasma deficiency of the von Willebrand factor cleaving metalloprotease A Disintegrin And Metalloprotease with ThromboSpondin 1 repeats (ADAMTS13), a number of laboratory assays for measuring ADAMTS13 and related autoantibodies have been developed. Current knowledge on the diagnostic and prognostic value of ADAMTS13 and anti-ADAMTS13 assays is summarized in this review. Copyright ÂEntities:
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Year: 2012 PMID: 22244722 DOI: 10.1016/j.lpm.2011.10.025
Source DB: PubMed Journal: Presse Med ISSN: 0755-4982 Impact factor: 1.228