Delayed diagnosis of congenital thrombotic thrombocytopenic purpura in a patient with recurrent strokes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Hematology
Link
https://link.springer.com/content/pdf/10.1007/s11239-021-02629-7.pdf
Reference14 articles.
1. Kokame K, Matsumoto M, Soejima K et al (2002) Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci USA 99(18):11902–11907
2. Remuzzi G, Galbusera M, Noris M et al (2002) von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. Blood 100(3):778–785
3. Alwan F, Vendramin C, Liesner R et al (2019) Characterization and treatment of congenital thrombotic thrombocytopenic purpura. Blood 133(15):1644–1651
4. Kremer Hovinga JA, George JN (2019) Hereditary thrombotic thrombocytopenic purpura. N Engl J Med 381(17):1653–1662
5. Sonneveld MA, de Maat MP, Portegies ML et al (2015) Low ADAMTS13 activity is associated with an increased risk of ischemic stroke. Blood 126(25):2739–2746. https://doi.org/10.1182/blood-2015-05-643338
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