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P-50 Hereditary angioedema breakthrough: FXII mutation discovery and the power of Icatibant and Lanadelumab Aviv Talmon, Limor Rubin, Yaarit Ribak, Oded Shamriz, Mariana Druker, Inon Sarig, Eyal Ben Dori, Yuval Tal Allergy and Clinical Immunology Unit, Department of Medicine, Hadassah Medical Organization, Faculty of Medicine, Hebrew University of Jerusalem, Israel Allergy, Asthma & Clinical Immunology 2025, 21(Suppl 2) :P-50 Background, Objectives: Hereditary angio-edema (HAE) is a rare, life-threatening disorder characterized by recurrent angioedema episodes

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It may be a sign of a urinary tract infection, dehydration, kidney stones, sexually transmitted diseases or other health conditions

At Centra Internal Medicine, we help you manage these symptoms, and most patients find that they improve as the body adjusts to the medication

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