Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency—Experience From the Hungarian Angioedema Center of Reference and Excellence

BACKGROUND: Hereditary Angioedema with C1-inhibitor deficiency (C1-INH-HAE) is a rare disease characterized by recurrent subcutaneous and/or submucosal edematous (HAE) episodes, which may occur at any age. The mean age of the symptom onset is 10–12 years. Diagnostic protocols differ by age group and...

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Detalles Bibliográficos
Autores principales: Andrási, Noémi, Balla, Zsuzsanna, Visy, Beáta, Szilágyi, Ágnes, Csuka, Dorottya, Varga, Lilian, Farkas, Henriette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Allergy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234934/
https://www.ncbi.nlm.nih.gov/pubmed/35769571
http://dx.doi.org/10.3389/falgy.2022.860355

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234934/
https://www.ncbi.nlm.nih.gov/pubmed/35769571
http://dx.doi.org/10.3389/falgy.2022.860355

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