Description
Thrombotic thrombocytopenic purpura (TTP) is a disease characterized by a decrease in the activity of the ADAMTS13 enzyme, which is involved in the cleavage of von Willebrand factor multimers, resulting in the persistence of the latter and spontaneous platelet aggregation. TTP is characterized by non-immune microangiopathic hemolytic anemia, non-immune consumption thrombocytopenia, fever, renal failure, and neurological disorders.
Period of execution
Within 11 days. The specified time does not include the day of biomaterial collection
Biomaterial type