Pediatric hereditary angioedema due to C1-inhibitor deficiency
<p>Abstract</p> <p>Hereditary angioedema (HAE) resulting from the deficiency of the C1 inhibitor (C1-INH) is a rare, life-threatening disorder. It is characterized by attacks of angioedema involving the skin and/or the mucosa of the upper airways, as well as the intestinal mucosa....
Main Author: | Farkas Henriette |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2010-07-01
|
Series: | Allergy, Asthma & Clinical Immunology |
Online Access: | http://www.aacijournal.com/content/6/1/18 |
Similar Items
-
Ecallantide is a novel treatment for attacks of hereditary angioedema due to C1 inhibitor deficiency
by: Farkas H, et al.
Published: (2011-05-01) -
Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency
by: Stefania Loffredo, et al.
Published: (2018-07-01) -
The genetic basis of C1 inhibitor deficiency and hereditary angioedema
by: Cumming, S. A.
Published: (2002) -
A novel deep intronic SERPING1 variant as a cause of hereditary angioedema due to C1-inhibitor deficiency
by: Sofia Vatsiou, et al.
Published: (2020-07-01) -
Recurrent Angioedema with Abdominal and Genital Involvement in Childhood: Hereditary Angioedema Type 2 Disease due to C1 Inhibitor Functional Deficiency
by: Öner Özdemir, et al.
Published: (2020-03-01)