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Diagnosis and screening of patients with hereditary angioedema in primary care

Hereditary angioedema (HAE) is a rare autosomal dominant disease that commonly manifests with episodes of cutaneous or submucosal angioedema and intense abdominal pain. The condition usually presents due to a deficiency of C1 esterase inhibitor (C1-INH) that leads to the overproduction of bradykinin...

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Detalles Bibliográficos
Autores principales: Henao, Maria Paula, Kraschnewski, Jennifer L, Kelbel, Theodore, Craig, Timothy J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859422/
https://www.ncbi.nlm.nih.gov/pubmed/27194914
http://dx.doi.org/10.2147/TCRM.S86293

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