Fibrinogen Longmont: A Clinically Heterogeneous Dysfibrinogenemia with Discrepant Fibrinogen Results Influenced by Clot Detection Method and Reagent
- PMID: 35088022
- PMCID: PMC8786559
- DOI: 10.1055/s-0041-1740644
Fibrinogen Longmont: A Clinically Heterogeneous Dysfibrinogenemia with Discrepant Fibrinogen Results Influenced by Clot Detection Method and Reagent
Conflict of interest statement
Conflict of Interest None declared.
References
-
- Subcommittee on Factor XIII and Fibrinogen . Casini A, Undas A, Palla R, Thachil J, de Moerloose P. Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH. J Thromb Haemost. 2018;16(09):1887–1890. - PubMed
-
- Casini A, Neerman-Arbez M, Ariëns R A, de Moerloose P. Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management. J Thromb Haemost. 2015;13(06):909–919. - PubMed
-
- Hill M, Dolan G. Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias. Haemophilia. 2008;14(05):889–897. - PubMed
-
- Lefkowitz J B, DeBoom T, Weller A, Clarke S, Lavrinets D. Fibrinogen Longmont: a dysfibrinogenemia that causes prolonged clot-based test results only when using an optical detection method. Am J Hematol. 2000;63(03):149–155. - PubMed
-
- Lounes K C, Lefkowitz J B, Coates A I, Hantgan R R, Henschen-Edman A, Lord S T. Fibrinogen Longmont. A heterozygous abnormal fibrinogen with B beta Arg-166 to Cys substitution associated with defective fibrin polymerization. Ann N Y Acad Sci. 2001;936:129–132. - PubMed
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