Factor XI gene analysis in thrombophilia and factor XI deficiency
โ Scribed by Victor E. A. Gerdes; Roderik A. Kraaijenhagen; Esther W. M. Vogels; Hugo Ten Cate; Pieter H. Reitsma
- Book ID
- 109148357
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 356 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1538-7933
No coin nor oath required. For personal study only.
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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
## sor of Medicine and Biochemistry. The subject of today's conference is factor XI deficiency and hemostasis. First, I would like to present two patients with factor XI deficiency and discuss their evaluation and management since the problems posed by these two patients focus on the biological ro