Outcomes of long term treatments of type I hereditary angioedema in a Turkish family
ANAIS BRASILEIROS DE DERMATOLOGIA, vol.92, no.5, pp.654-659, 2017 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 92 Issue: 5
- Publication Date: 2017
- Doi Number: 10.1590/abd1806-4841.20175899
- Journal Name: ANAIS BRASILEIROS DE DERMATOLOGIA
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.654-659
- Keywords: Complement CI inhibitor protein, Danazol, Hereditary Angioedema Types I and II, C1 INHIBITOR GENE, DANAZOL TREATMENT, ATTENUATED ANDROGENS, THROMBOSIS, MUTATION, ATTACKS, PROPHYLAXIS, CONCENTRATE, DEFICIENCY, EDEMA
- Karadeniz Technical University Affiliated: Yes
Abstract
BACKGROUND: Hereditary angioedema is a rare autosomal dominantly inherited immunodeficiency disorder characterized by potentially life-threatening angioedema attacks.