Where we are with acquired angioedema due to C1 inhibitor deficiency: A systematic literature review.
Sign Up to like & getrecommendations! Published in 2021 at "Clinical immunology"
DOI: 10.1016/j.clim.2021.108819
Abstract: Acquired angioedema due to C1 inhibitor deficiency (C1-INH-AAE) is a rare disease characterized by adult-onset recurrent non-urticarial angioedema with low levels of C1-INH. It is associated with lymphoproliferative disorders, and treatments are off-label with variable… read more here.
Keywords: inh aae; angioedema due; inhibitor deficiency; acquired angioedema ... See more keywords
Emerging drugs for the treatment of hereditary angioedema due to C1-inhibitor deficiency
Sign Up to like & getrecommendations! Published in 2022 at "Expert Opinion on Emerging Drugs"
DOI: 10.1080/14728214.2022.2105834
Abstract: ABSTRACT Introduction Hereditary angioedema due to C1-inhibitor (C1-INH-HAE) is a rare disease characterized by unpredictable swelling attacks that may be life-threatening when affecting the upper airways. Understanding the pathophysiology of HAE and the mechanism of… read more here.
Keywords: hereditary angioedema; angioedema; emerging drugs; angioedema due ... See more keywords
Psychometric study of the SF-36v2 in hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE)
Sign Up to like & getrecommendations! Published in 2022 at "Orphanet Journal of Rare Diseases"
DOI: 10.1186/s13023-022-02202-2
Abstract: Background The generic 36-item Short-Form Health Survey (SF-36v2) has been used to assess health related quality of life in adult patients with hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) even though it has not yet… read more here.
Keywords: inhibitor deficiency; due inhibitor; inh hae; hereditary angioedema ... See more keywords
HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY IN PEDIATRIC PATIENTS IN CROATIA – FIRST NATIONAL STUDY, DIAGNOSTIC AND PROPHYLACTIC CHALLENGES
Sign Up to like & getrecommendations! Published in 2019 at "Acta Clinica Croatica"
DOI: 10.20471/acc.2019.58.01.18
Abstract: SUMMARY Hereditary angioedema (HAE) is a rare autosomal dominant disease with deficiency (type I) or dysfunction (type II) of C1 inhibitor, caused by mutations in the C1-INH gene, characterized by recurrent submucosal or subcutaneous edemas… read more here.
Keywords: study; hereditary angioedema; deficiency; pediatric patients ... See more keywords