HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY IN PEDIATRIC PATIENTS IN CROATIA – FIRST NATIONAL STUDY, DIAGNOSTIC AND PROPHYLACTIC CHALLENGES

Hereditary angioedema (HAE) is a rare autosomal dominant disease with deficiency (type I) or dysfunction (type II) of C1 inhibitor, caused by mutations in the C1-INH gene, characterized by recurrent submucosal or subcutaneous edemas including skin swelling, abdominal pain and life-threatening episod...

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Detalles Bibliográficos
Autores principales: Karadža-Lapić, Ljerka, Barešić, Marko, Vrsalović, Renata, Ivković-Jureković, Irena, Sršen, Saša, Prkačin, Ingrid, Rijavec, Matija, Cikojević, Draško
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sestre Milosrdnice University Hospital and Institute of Clinical Medical Research, Vinogradska cesta c. 29 Zagreb 2019
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629194/
https://www.ncbi.nlm.nih.gov/pubmed/31363336
http://dx.doi.org/10.20471/acc.2019.58.01.18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629194/
https://www.ncbi.nlm.nih.gov/pubmed/31363336
http://dx.doi.org/10.20471/acc.2019.58.01.18

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