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...

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Bibliographic Details
Main Authors: Lubna Foad Hussain, Obeida Amir Abid
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
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