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Laboratory Diagnosis of Von Willebrand Disease
Von Willebrand disease (vWD) is the most frequently inherited bleeding disorder and affects 1% of the general population. Laboratory testing plays a critical role in diagnosis/classification and guides clinical management. In this presentation, the genetic causes of von Willebrand disease, the common laboratory assays used to diagnose vWD, and common subtypes of vWD are discussed.
Originally presented on March 18, 2013, in Salt Lake City, Utah.
Lecture Presenter
 | Delu Zhou MD, PhD Pathology Resident |
Delu Zhou graduated from Hebei Medical University (medical training) and Indiana University (PhD training in immunology) and worked in a postdoc fellowship at the University of California, San Francisco studying innate immunity and autoimmune diseases prior to joining the residency program at University of Utah.
Objectives
After this presentation, participants will be able to:
- Explain common symptoms and genetic causes of von Willebrand disease.
- Describe the common laboratory assays used to diagnose von Willebrand disease.
- List common subtypes of von Willebrand disease.
Sponsored by:
University of Utah School of Medicine, and ARUP Laboratories