Hereditary Angioedema and Gastrointestinal Complications: An Extensive Review of the Literature

Hereditary Angioedema (HAE) is a rare autosomal dominant (AD) disease characterized by deficient (type 1) or nonfunctional (type 2) C1 inhibitor protein. The disorder is associated with episodes of angioedema of the face, larynx, lips, abdomen, or extremities. The angioedema is caused by the activat...

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Detalles Bibliográficos
Autores principales: Patel, Napoleon, Suarez, Lisbet D., Kapur, Sakshi, Bielory, Leonard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4538593/
https://www.ncbi.nlm.nih.gov/pubmed/26339513
http://dx.doi.org/10.1155/2015/925861

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4538593/
https://www.ncbi.nlm.nih.gov/pubmed/26339513
http://dx.doi.org/10.1155/2015/925861

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