von Willebrand disease type1/type 2N compound heterozygotes: diagnostic and management challenges

Br J Haematol. 2017 Mar;176(6):994-997. doi: 10.1111/bjh.14028. Epub 2016 Mar 11.

Authors

Juliana Perez Botero¹, Rajiv K Pruthi^{1

2}, William L Nichols^{1

2}, Aneel A Ashrani^{1

2}, Mrinal M Patnaik¹

Affiliations

¹ Division of Hematology, Mayo Clinic, Rochester, MN, USA.
² Special Coagulation Laboratory, Division of Hematopathology, Mayo Clinic, Rochester, MN, USA.

PMID: 26970096
DOI: 10.1111/bjh.14028

No abstract available

Keywords: bleeding; factor VIII; genetics of thrombosis and haemostasis; von Willebrand disease; von Willebrand factor.

Publication types

Letter

MeSH terms

Adult
Aged
Female
Heterozygote
Humans
Male
Young Adult
von Willebrand Diseases / diagnosis*
von Willebrand Diseases / pathology
von Willebrand Diseases / therapy*