Congenital von Willebrand factor deficiency in single Iraqi teaching hospital: A descriptive study
Background: Von Willebrand disease (vWD) is a common, inherited hemorrhagic disorder caused by a deficiency or dysfunction of the protein von Willebrand factor (vWF). Objectives: The aim of this study is to assess the diagnosis and treatment of vWD in a single Iraqi teaching hospital. Patients and...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2016-01-01
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Series: | Iraqi Journal of Hematology |
Subjects: | |
Online Access: | http://www.ijhonline.org/article.asp?issn=2072-8069;year=2016;volume=5;issue=2;spage=154;epage=156;aulast=Hussain |