Consensus on diagnosis and management of Hereditary Angioedema in the Middle East: A Delphi initiative

BACKGROUND: Hereditary angioedema (HAE), a potentially life-threatening genetic disorder due to C1 inhibitor deficiency in most cases, is characterized by sudden and/or recurrent attacks of angioedema (subcutaneous/submucosal swellings). The global World Allergy Organization (WAO)/European Academy o...

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Detalles Bibliográficos
Autores principales: Maurer, Marcus, Abuzakouk, Mohamed, Al-Ahmad, Mona, Al-Herz, Waleed, Alrayes, Hassan, Al-Tamemi, Salem, Arnaout, Rand, Binghadeer, Hend, Gutta, Ravi, Irani, Carla, Mobayed, Hassan, Nasr, Iman, Shendi, Hiba, Zaitoun, Fares
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Allergy Organization 2022
Materias:
Full-Length Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803817/
https://www.ncbi.nlm.nih.gov/pubmed/36601261
http://dx.doi.org/10.1016/j.waojou.2022.100729

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803817/
https://www.ncbi.nlm.nih.gov/pubmed/36601261
http://dx.doi.org/10.1016/j.waojou.2022.100729

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