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[Hereditary angioedema]. / Hereditäres Angioödem.
Aygören-Pürsün, Emel; Bork, Konrad.
Afiliação
  • Aygören-Pürsün E; Angioödem-Ambulanz und Comprehensive Care Center für hereditäres Angioödem, Klinik für Kinder- und Jugendmedizin, Universitätsklinikum Frankfurt, Goethe-Universität, Theodor-Stern-Kai 7, 60590, Frankfurt am Main, Deutschland. aygoeren@em.uni-frankfurt.de.
  • Bork K; Hautklinik, Universitätsmedizin Mainz, Langenbeckstr. 1, 55131, Mainz, Deutschland.
Internist (Berl) ; 60(9): 987-995, 2019 Sep.
Article em De | MEDLINE | ID: mdl-31363809
Hereditary angioedema (HAE) encompasses a heterogeneous group of diseases with similar phenotypes but different underlying genotypes. Specific clinical signs may point to HAE as opposed to histaminergic angioedema: the typical prolonged development of angioedema over time, positive family history, a lack of response to antihistamines and steroids and response to bradykinin antagonists are typical signs of HAE. The different types of HAE may be associated with a severe clinical course. They are life-long conditions and are still potentially life-threatening. The quality of life of patients with HAE may be considerably impaired. Management plans should be individualized, which is facilitated by the variety of specific medicastions available.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator XII / Bradicinina / Fator XIIa / Proteína Inibidora do Complemento C1 / Angioedemas Hereditários Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: De Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator XII / Bradicinina / Fator XIIa / Proteína Inibidora do Complemento C1 / Angioedemas Hereditários Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: De Ano de publicação: 2019 Tipo de documento: Article