Conditions / Genetic

factor X deficiency

info ยท Genetic

A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood.

Signs and symptoms

  • Prolonged prothrombin time
  • Reduced factor X activity
  • Prolonged bleeding after surgery
  • Menorrhagia
  • Intramuscular hematoma
  • Joint hemorrhage
  • Intracranial hemorrhage
  • Epistaxis
  • Gingival bleeding
  • Prolonged partial thromboplastin time

Also known as: disease, Stuart-Prower