Literature DB >> 24706524

Co-inheritance of mild hemophilia A and heterozygosity for type 2N von Willebrand disease: a diagnostic and therapeutic challenge.

Holly Lindsay1, Katie Bergstrom, Lakshmi Srivaths.   

Abstract

Hemophilia A and von Willebrand disease are the two most common inherited bleeding disorders. Despite their frequency, however, there are very few reports of co-inheritance of the two disorders. We present the first report of a patient with mild hemophilia A and heterozygosity for type 2N von Willebrand disease (VWD). We discuss the patient's phenotype and highlight the diagnostic and therapeutic challenges caused by this co-inheritance.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  bleeding disorders; hemophilia A; type 2N; von Willebrand disease

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Year:  2014        PMID: 24706524     DOI: 10.1002/pbc.25054

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  1 in total

1.  Life-threatening bleeding in a patient with mild hemophilia A and heterozygosity for von Willebrand disease Type 2N.

Authors:  John N Allan; Kenneth D Friedman; Maria T DeSancho
Journal:  Int J Hematol       Date:  2014-09-12       Impact factor: 2.490

  1 in total

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