Abstract
Hereditary Angioedema is a rare condition characterized by episodes of angioedema without urticaria in the skin or mucosal tissues due to a C1 Esterase Antigen or Functional Deficiency. Patients with this condition may present with symptoms of abdominal pain, nausea, vomiting, diarrhea, and even circulatory shock that may be misdiagnosed as other pathologies.
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