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Article

Hereditary angioedema: the challenges of cross-border family investigation and treatment.

BMJ case reports - 14 Apr 2020

Brix Anna Trier Heiberg, Svensson Trine Mehlbye, Sandberg Malin, Bygum Anette

Abstract excerpt

Hereditary angioedema (HAE) is a rare genetic disorder characterised by recurrent swellings involving subcutaneous and submucosal tissue that can be potentially life threatening in cases involving the upper airway. In this case report, we present a Syrian refugee family with HAE who have lived in Denmark since 2014. The index patient is an 8-year-old girl diagnosed with HAE after being hospitalised in Denmark...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 32295794
DOI: 10.1136/bcr-2019-231906
PMCID: PMC7199096

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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