RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164070048
T1 Fibrin Stabilizing Factor (Factor XIII) Deficiency
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164070048
RD 2024/04/18
AB Inherited  coagulation  disorder  resulting  in  life-long  bleeding  tendency  in  homozygotes  with  poor  wound  healing  and  easy  bruising.  The  presence  of  severe  bleeding  diathesis  is  characterized  by  recurrent  soft  tissue  bleeding,  poor  wound  healing,  and  a  high  incidence  of  intracranial  hemorrhage.  The  presence  of  normal  coagulation  screening  tests,  including  prothrombin  time  (PT),  partial  thromboplastin  time  (PTT),  fibrinogen  level,  platelet  count,  and  bleeding  time  and  a  history  of  severe  bleeding  diathesis  should  be  considered  a  Factor  XIII  deficiency  until  proven  otherwise.