Literature DB >> 15596404

Current and future therapy for hereditary angioedema.

Bruce L Zuraw1.   

Abstract

Hereditary angioedema (HAE) is an autosomal dominant disease characterized by recurrent episodes of potentially life-threatening angioedema. Attacks of angioedema in HAE patients typically last 3 or more days, begin during childhood, and continue to occur throughout life. Tragically, patients with HAE continue to die as a direct consequence of the disease. Minimizing the morbidity and mortality associated with HAE requires both effective treatment of acute attacks as well as strategies to prevent HAE attacks. While there is currently no effective therapy available in the United States for the treatment of acute attacks of HAE, several molecules have demonstrated impressive efficacy in this setting, and it is likely that one or more of these new drugs will become available in the United States soon. This article will review both the current and the future therapeutic options for the treatment of HAE.

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Year:  2005        PMID: 15596404     DOI: 10.1016/j.clim.2004.08.001

Source DB:  PubMed          Journal:  Clin Immunol        ISSN: 1521-6616            Impact factor:   3.969


  7 in total

Review 1.  Current and emerging management options for hereditary angioedema in the US.

Authors:  Tolly G Epstein; Jonathan A Bernstein
Journal:  Drugs       Date:  2008       Impact factor: 9.546

Review 2.  Angioedema with normal laboratory values: the next step.

Authors:  Janelle Sher; Mark Davis-Lorton
Journal:  Curr Allergy Asthma Rep       Date:  2013-10       Impact factor: 4.806

Review 3.  Pediatric hereditary angioedema.

Authors:  Andrew J MacGinnitie
Journal:  Pediatr Allergy Immunol       Date:  2013-12-09       Impact factor: 6.377

4.  Complement 4 levels of a 4-year-old girl with angioedema.

Authors:  Soyoung Shin; Yoon Tae Lee; Kyung Yil Lee; Joonhong Park; Jae Ho Lee; Eun Ae Yang
Journal:  Clin Exp Pediatr       Date:  2019-11-08

5.  Oral Surgery Procedures in a Patient Affected by Hereditary Angioedema Type I.

Authors:  Chiara Cinquini; Simonetta Santarelli; Alberto Marianelli; Marco Nisi; Mario Gabriele; Antonio Barone
Journal:  Case Rep Dent       Date:  2022-01-29

6.  Recent developments in the treatment of acute abdominal and facial attacks of hereditary angioedema: focus on human C1 esterase inhibitor.

Authors:  Lourdes Pastó Cardona; Ramon Lleonart Bellfill; Joaquim Marcoval Caus
Journal:  Appl Clin Genet       Date:  2010-12-03

7.  The establishment and utility of Sweha-Reg: a Swedish population-based registry to understand hereditary angioedema.

Authors:  Lotus Mallbris; Patrik Nordenfelt; Janne Björkander; Anders Lindfors; Sonja Werner; Carl-Fredrik Wahlgren
Journal:  BMC Dermatol       Date:  2007-11-30
  7 in total

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