How physicians approach hereditary angioedema: a single center study

BACKGROUND: Hereditary angioedema (HAE) is a rare autosomal dominant disorder caused by C1-inhibitor deficiency. It is characterized by recurrent attacks of cutaneous and upper respiratory tract swelling, and abdominal pain due to mucosal edema. Early detection and treatment prevent unnecessary inte...

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Detalles Bibliográficos
Autores principales: Terzioglu, Kadriye, Ediger, Dane, Ozdemir, Ebru, TulumenOzturk, Raziye, Dogan, Fatma Oflu, Sancar, Ozgur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asia Pacific Association of Allergy, Asthma and Clinical Immunology 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669465/
https://www.ncbi.nlm.nih.gov/pubmed/36452014
http://dx.doi.org/10.5415/apallergy.2022.12.e40

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669465/
https://www.ncbi.nlm.nih.gov/pubmed/36452014
http://dx.doi.org/10.5415/apallergy.2022.12.e40

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