Abstract
Von Willebrand disease (VWD) is the most common inherited bleeding disorder, and one of the most complex. It is caused primarily by defects in the von Willebrand factor (VWF) protein, and can be divided into both quantitative and qualitative disorders. The current classification system considers type 1 VWD to represent the mild to moderate quantitative deficiencies of VWF, and type 3 VWD to represent the severe quantitative deficiency of VWF. Type 2 refers to the qualitative variants which are divided by VWF defect. Appropriate classification of VWD is important to determine the most appropriate treatment for affected patients.
Original language | English (US) |
---|---|
Title of host publication | Textbook of von Willebrand Disease |
Subtitle of host publication | Basic and Clinical Aspects |
Publisher | wiley |
Pages | 73-79 |
Number of pages | 7 |
ISBN (Electronic) | 9781119419525 |
ISBN (Print) | 9781119419488 |
DOIs | |
State | Published - Jan 1 2024 |
Keywords
- bleeding
- factor VIII
- genetics
- platelets
- Von Willebrand disease
- von Willebrand factor
ASJC Scopus subject areas
- General Medicine