RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164072422
T1 Hemophilia A
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164072422
RD 2024/04/19
AB Most  severe  hereditary  coagulation  disorder.  It  is  caused  by  defective  synthesis  of  plasma  protein  factor  VIII.  The  condition  must  be  suspected  in  the  presence  of  prolonged  bleeding  following  a  venepuncture  or  simple  heel  prick  at  the  time  of  birth.