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Diabetes (2002) 51:294450

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

Some individuals lose weight more quickly, while others progress at a slower pace

Niemoeller, E