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