Alpha-2-plasmin inhibitor deficiency

Congenital alpha2 antiplasmin deficiency is a rare hemorrhagic disorder caused by congenital deficiency of alpha2 antiplasmin, leading to dysregulated fibrinolysis and is characterized by a hemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes (often in unusual locations like diaphysis of long bones). Congenital alpha2 antiplasmin deficiency is inherited in an autosomal recessive manner.

Also known as: alpha-2-plasmin inhibitor deficiency, plasmin inhibitor deficiency, anti-plasmin deficiency, congenital, antiplasmin deficiency, antiplasmin deficiency, congenital, congenital alpha2-antiplasmin deficiency

12 clinical trials for this condition and its sub-types, 0 tagged with Alpha-2-plasmin inhibitor deficiency itself.