Clinical manifestations of hereditary angioedema: a systematic review of treatment

Abstract excerpt

<title>Abstract</title> <p>Hereditary Angioedema or HAE is a rare autosomal dominant disease leading to three major types of acute swelling and is known to be triggered by C1 esterase inhibitor deficiency. The purpose of this systematic review was to summarize the key clinical features of HAE and to compare and analyze the available management options and potential new management prospects. For this study, their...

Topics

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• Angioedema
• Angioedemas, Hereditary
• Bradykinin
• Child
• Child, Preschool
• Coagulation, Bradykinin, Polyphosphates, and Angioedema
• Complement C1 Inhibitor Protein
• Mutation

Identifiers and source

Literature Corpus work

1bca2ef1-6d3c-541c-bb72-1d293d4edc78

DOI

10.21203/rs.3.rs-6245901/v1