Survey of actual conditions of erythema marginatum as a prodromal symptom in Japanese patients with hereditary angioedema

BACKGROUND: Hereditary angioedema (HAE) is a rare but life-threatening condition. HAE types I and II (HAE-1/2) result from C1-inhibitor (C1–INH) deficiency. However, recent genetic analysis has established a new type of HAE with normal C1–INH (HAEnC1-INH). The mutations of factor XII, plasminogen, a...

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Detalles Bibliográficos
Autores principales: Ohsawa, Isao, Fukunaga, Atsushi, Imamura, Shinya, Iwamoto, Kazumasa, Tanaka, Akio, Hide, Michihiro, Honda, Daisuke, Yamashita, Kouhei, Fujiwara, Chisako, Ishikawa, Osamu, Yamaguchi, Takeo, Maehara, Junichi, Hirose, Tomoya, Ieko, Masahiro, Umekita, Kunihiko, Nakamura, Yuya, Gotoh, Hiromichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: World Allergy Organization 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872976/
https://www.ncbi.nlm.nih.gov/pubmed/33643518
http://dx.doi.org/10.1016/j.waojou.2021.100511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872976/
https://www.ncbi.nlm.nih.gov/pubmed/33643518
http://dx.doi.org/10.1016/j.waojou.2021.100511

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