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P-04 Hereditary angioedema due to factor XII mutation: Clinical manifestations among males subjects Delphine Gobert 1,* , Btisseme Ahouach 1 , Isabelle Boccon-Gibod 2 , Laurence Bouillet 2 , Aurlie Du-Thanh 3 , David Launay 4 , Ludovic Martin 5 , Gaelle Hardy 6 , Olivier Fain 1 1 Sorbonne Universit, internal medicine department, University Hospital Saint-Antoine, Assistance Publique-Hpitaux de Paris, Paris, France

A previous study compared the efficacy and tolerability of an initial combination therapy with vildagliptin/pioglitazone to component monotherapy [20]

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Medication can be a useful tool for the right patient, but sustainable outcomes require follow-up, nutrition planning, activity support, lab monitoring, and a practical maintenance strategy