A rare presentation of homozygous factor X deficiency in a pregnant patient: A case report and review of the literature
Author:
Affiliation:
1. Universitaire Ziekenhuizen Leuven; Leuven Belgium
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.13654/fullpdf
Reference12 articles.
1. Recessively inherited coagulation disorders;Mannucci;Blood,2004
2. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders;Peyvandi;J Thromb Haemost,2012
3. Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era;Girolami;Haemophilia,2011
4. A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders;Simeoni;Blood,2016
5. Molecular defect (Gla+14Lys) and its functional consequences in a hereditary factor X deficiency (Factor X “Vorarlberg”);Watzke;J Biol Chem,1990
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1. A Compound Heterozygosis of Two Novel Mutations Causes Factor X Deficiency in a Chinese Pedigree;Acta Haematologica;2020-06-29
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