Hereditary angioedema (HAE) is a relatively rare disease, with an estimated prevalence of approximately 1 per 50,000 in the general population. Despite its rarity, HAE has become an area of intense interest within the medical community. This interest likely reflects several different aspects of HAE, including: the high potential for significant morbidity and mortality associated with attacks of angioedema in HAE patients, the frequent failure to make an accurate and timely diagnosis, the progress in unraveling the underlying pathophysiology of HAE, and the tremendous advances in treatment options. To limit the morbidity and mortality that has long afflicted patients with HAE, it has become increasingly important that the clinician understand both the underlying mechanisms of swelling in HAE and the newer treatment strategies that have been developed for HAE. This supplement contains 3 reviews that summarize the current state-of-the-art regarding the pathophysiology and treatment of HAE.
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