Conditions / Genetic
alpha-2-plasmin inhibitor deficiency
info · Genetic · ICD-10: D68.8
A hemorrhagic disease that has_material_basis_in mutation in the PLI gene. It is characterized by a hemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes.
Signs and symptoms
- Hemothorax
- Bruising susceptibility
- Joint hemorrhage
- Persistent bleeding after trauma
Also known as: antiplasmin defiency; plasmin inhibitor deficiency