RT Book, Section
A1 Clare, Jonathan A. Drew
A1 Hemphill, Robin R.
A2 Tintinalli, Judith E.
A2 Ma, O. John
A2 Yealy, Donald M.
A2 Meckler, Garth D.
A2 Stapczynski, J. Stephan
A2 Cline, David M.
A2 Thomas, Stephen H.
SR Print(0)
ID 1166812679
T1 Hemophilias and von Willebrand’s Disease
T2 Tintinalli's Emergency Medicine: A Comprehensive Study Guide, 9e
YR 2020
FD 2020
PB McGraw-Hill Education
PP New York, NY
SN 9781260019933
LK accessemergencymedicine.mhmedical.com/content.aspx?aid=1166812679
RD 2024/04/20
AB Hemophilias  are  bleeding  disorders  due  to  deficiency  in  clotting  cascade  factors  (see  Chapter  232,  “Hemostasis”).1-3  The  most  common  factor  abnormalities  are  of  factor  VIII  (hemophilia  A)  or  factor  IX  (hemophilia  B).  von  Willebrand’s  disease  is  a  related  defect  of  the  von  Willebrand  factor.4