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Article

Management of hereditary angioedema type I and homozygous MTHFR mutation during pregnancy.

Allergologia et immunopathologia - 1 Jan 2021

Batlle Amanda Ribeiro, do Carmo Ana Paula Possar, Galao Nirelcio, Grumach Anete S

Abstract excerpt

Hereditary angioedema (HAE) is an autosomal dominant disease, characterized by edema attacks resulting from quantitative and/or functional deficiency of the C1 inhibitor (C1-INH), which acts in controlling the complement, coagulation, fibrinolysis, and contact systems. The exacerbation of these systems results in decreased circulating levels of kallikrein and conversion of bradykinin. In addition, thrombophilia...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 34224212
DOI: 10.15586/aei.v49i4.57

Provenance

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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