Management of pregnancy complications in type 2N von Willebrand disease associated to a novel mutation

Haemophilia. 2018 May;24(3):e148-e152. doi: 10.1111/hae.13481. Epub 2018 Apr 14.

Authors

Y Brennan¹, E J Favaloro^{2

3}, J Curtin^{4

5}, J Curnow^{1

3

5}

Affiliations

¹ Department of Haematology, Westmead Hospital, Sydney, NSW, Australia.
² Diagnostic Haemostasis Laboratory, Laboratory Haematology, NSW Health Pathology, Westmead Hospital, Sydney, NSW, Australia.
³ Sydney Centres for Thrombosis and Haemostasis, Westmead, NSW, Australia.
⁴ Department of Haematology, The Children's Hospital at Westmead, Sydney, NSW, Australia.
⁵ Sydney Medical School, The University of Sydney, Sydney, NSW, Australia.

PMID: 29656540
DOI: 10.1111/hae.13481

No abstract available

Publication types

Letter

MeSH terms

Adolescent
Factor VIII / genetics*
Factor VIII / metabolism
Female
Hemorrhage
Humans
Mutation, Missense / genetics*
Pedigree
Pregnancy
Pregnancy Complications, Hematologic / diagnosis*
Pregnancy Complications, Hematologic / therapy
Protein Binding
Young Adult
von Willebrand Disease, Type 2 / diagnosis*
von Willebrand Disease, Type 2 / therapy
von Willebrand Factor / metabolism

Substances

von Willebrand Factor
Factor VIII