## Diagnosis of von Willebrand disease Type 2N (vWD 2N ), which mimics hemophilia A and its carrier state, is important for accurate genetic counseling and appropriate therapy. To make testing for the disorder more clinically applicable, we developed a simplified method for measurement of factor V
Further evidence for recessive inheritance of von willebrand disease with abnormal binding of von willebrand factor to factor VIII
✍ Scribed by M. F. Lopez-Fernandez; M. J. Blanco-Lopez; M. P. Castiñeira; J. Batlle
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 739 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0361-8609
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A patient with type 2N ("Normandy" variant) von Willebrands disease is described. Her von Willebrand factor level was borderline low, while her factor Vlll was markedly decreased to 7%. Her plasma von Wlliebrand factor demonstrated a decreased ability to complex with factor Vlll In vitro, binding le