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