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Article

Hereditary angioedema.

Journal of drugs in dermatology : JDD - 1 Oct 2006

Sachse Michael M, Khachemoune Amor, Guldbakke Kjetil K, Kirschfink Michael

Abstract excerpt

Hereditary angioedema (HAE) is a rare autosomal dominant disorder caused by a C1-inhibitor deficiency. It is characterized by potentially life-threatening recurrent episodes of angioedema of the skin and mucosa. Several recent studies have further elucidated the immunology of HAE implicating bradykinin, the key mediator of the contact system. This article reviews the pathophysiology, subtypes, and clinical...

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PMID: 17039649

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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