TTP or complement-mediated TMA or both? A rare diagnosis and report of a novel plasminogen gene variant
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00277-021-04589-7.pdf
Reference8 articles.
1. George JN, Nester CM (2014) Syndromes of thrombotic microangiopathy. N Engl J Med 371(7):654–666. https://doi.org/10.1056/nejmra1312353
2. Chiasakul T, Cuker A (2018) Clinical and laboratory diagnosis of TTP: an integrated approach. Hematol (United States) 1:530–538. https://doi.org/10.1182/asheducation-2018.1.530
3. Camilleri RS, Scully M, Thomas M et al (2012) A phenotype-genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom. J Thromb Haemost 10(9):1792–1801. https://doi.org/10.1111/j.1538-7836.2012.04852.x
4. Deal T, Kremer Hovinga JA, Marques MB, Adamski J (2013) Novel ADAMTS13 mutations in an obstetric patient with Upshaw-Schulman syndrome. J Clin Apher 28(4):311–316. https://doi.org/10.1002/jca.21251
5. Bu F, Maga T, Meyer NC et al (2014) Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome. J Am Soc Nephrol 25(1):55–64. https://doi.org/10.1681/ASN.2013050453
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