Noonan Syndrome: Partial factor XI deficiency
✍ Scribed by de Haan, M. ;Kamp, J. J. P. v. d. ;Briët, E. ;Dubbeldam, J. ;Optiz, John M. ;Reynolds, James F.
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 316 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0148-7299
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Factor XI (FXI) deficiency is an uncommon autosomally transmitted coagulopathy found predominantly in Jewish kindreds. It is associated with variable bleeding tendency that usually manifests after trauma, surgery, or other challenges to hemostasis. Therefore, women with FXI deficiency are at risk of
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