The physician and hereditary angioedema friend or foe: 62-year diagnostic delay and iatrogenic procedures

Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare autosomal dominant disease characterized by episodes of acute subcutaneous swelling, and/or recurrent severe abdominal pain. The dise...

from #Head and Neck by Sfakianakis via simeraentaxei on Inoreader https://ift.tt/2z2nEUc