Rare inherited diagnosis, characterized by accumulation of fluids outside of blood vessels, blocking normal flow of blood or lymphatic fluid and causing swelling of tissues. This is cause by a deficiency in of a protein called C1 esterase inhibitor which maintains normal flow of fluids through capillaries. Symptoms can include slow progressive swelling without urticaria that generally subsides over 48-72 hours, located in mouth, hands, feet, or abdomen.

Medication we use to treat/manage: