1.
Ugeskr Laeger
; 180(6)2018 02 05.
Article
in Danish
| MEDLINE
| ID: mdl-29429480
ABSTRACT
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.
Subject(s)
Hereditary Angioedema Type III , Complement C1 Inactivator Proteins/genetics , Complement C1 Inactivator Proteins/metabolism , Diagnosis, Differential , Hereditary Angioedema Type III/diagnosis , Hereditary Angioedema Type III/drug therapy , Hereditary Angioedema Type III/pathology , Hereditary Angioedema Type III/physiopathology , Humans , Pedigree
2.
Ugeskr Laeger
; 178(15)2016 04 11.
Article
in Danish
| MEDLINE
| ID: mdl-27094536
Subject(s)
Insulin Resistance/physiology , Skin Neoplasms , Female , Humans , Middle Aged , Skin Neoplasms/etiology , Skin Neoplasms/pathology
3.
Acta Derm Venereol
; 94(6): 719-20, 2014 Nov.
Article
in English
| MEDLINE
| ID: mdl-24691846