Targeted exome analysis in patients with rare bleeding disorders: data from the Rare Bleeding Disorders in the Netherlands study

Background: Rare coagulation factor deficiencies and disorders of fibrinolysis (defined as rare bleeding disorders [RBDs]) present with a heterogeneous bleeding phenotype, and bleeding severity is difficult to predict. Objectives: Describe underlying rare genetic variants in the Dutch RBD population and investigate the relationship between genotype, laboratory phenotype, and clinical phenotype. Methods: The Rare Bleeding Disorders in the Netherlands is a cross-sectional, nationwide study conducted between October 1, 2017, and November 30, 2019. Bleeding scores and blood samples were collected... Mehr ...

Verfasser: Willems, Sterre P.E.
Simons, Annet
Saes, Joline L.
Weiss, Marjan
Rijpma, Sanna
Schoormans, Selene
Meijer, Karina
Cnossen, Marjon H.
Schutgens, Roger E.G.
van Es, Nick
Nieuwenhuizen, Laurens
den Exter, Paul L.
Kruis, Ilmar C.
Blijlevens, Nicole M.A.
van Heerde, Waander L.
Schols, Saskia E.M.
Dokumenttyp: Artikel
Erscheinungsdatum: 2024
Schlagwörter: blood coagulation disorders / exome sequencing / fibrinolysis / hemostasis / inherited / Hematology
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29204001
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://dspace.library.uu.nl/handle/1874/455441