1.
Ugeskr Laeger
; 180(6)2018 02 05.
Artículo
en Danés
| MEDLINE
| ID: mdl-29429480
RESUMEN
Hereditary angio-oedema (HAE) is a rare, potentially fatal disease characterized by recurrent swelling of skin and mucosa. Besides HAE with quantitative (type I) or qualitative (type II) deficiency of complement C1-inhibitor (C1-INH), a new subtype of HAE is now described with normal levels of C1-INH. This subtype is possibly underdiagnosed, and a treatment regimen and general knowledge about the condition is still in its infancy. The purpose of this article is to inform Danish doctors about the disease to identify more Danish patients.
Asunto(s)
Angioedema Hereditario Tipo III , Proteínas Inactivadoras del Complemento 1/genética , Proteínas Inactivadoras del Complemento 1/metabolismo , Diagnóstico Diferencial , Angioedema Hereditario Tipo III/diagnóstico , Angioedema Hereditario Tipo III/tratamiento farmacológico , Angioedema Hereditario Tipo III/patología , Angioedema Hereditario Tipo III/fisiopatología , Humanos , Linaje
2.
Ugeskr Laeger
; 178(15)2016 04 11.
Artículo
en Danés
| MEDLINE
| ID: mdl-27094536
3.
Acta Derm Venereol
; 94(6): 719-20, 2014 Nov.
Artículo
en Inglés
| MEDLINE
| ID: mdl-24691846