A Comprehensive Management Approach in Pediatric and Adolescent Patients With Hereditary Angioedema

Hereditary angioedema (HAE) is a rare autosomal-dominant disorder; most cases are characterized by low plasma levels of C1 esterase inhibitor (C1-INH). Clinical manifestations of HAE due to C1-INH deficiency include unpredictable, acute, recurrent episodes of nonpruritic swelling that can affect the...

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Detalles Bibliográficos
Autores principales: Tachdjian, Raffi, Kaplan, Allen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478326/
https://www.ncbi.nlm.nih.gov/pubmed/36908071
http://dx.doi.org/10.1177/00099228231155703

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478326/
https://www.ncbi.nlm.nih.gov/pubmed/36908071
http://dx.doi.org/10.1177/00099228231155703

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