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Pediatric hereditary angioedema: an update
Hereditary angioedema (HAE) with C1-inhibitor (C1-Inh) deficiency (C1-Inh-HAE) is a rare, life-threatening, and disabling genetic disorder characterized by self-limited tissue swelling caused by deficiency or dysfunction of C1-Inh. Our aim in this update is to discuss new advances in HAE therapy, fo...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000Research
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531155/ https://www.ncbi.nlm.nih.gov/pubmed/28781749 http://dx.doi.org/10.12688/f1000research.11320.1 |
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author | Sabharwal, Geetika Craig, Timothy |
author_facet | Sabharwal, Geetika Craig, Timothy |
author_sort | Sabharwal, Geetika |
collection | PubMed |
description | Hereditary angioedema (HAE) with C1-inhibitor (C1-Inh) deficiency (C1-Inh-HAE) is a rare, life-threatening, and disabling genetic disorder characterized by self-limited tissue swelling caused by deficiency or dysfunction of C1-Inh. Our aim in this update is to discuss new advances in HAE therapy, focusing mainly on the various treatment options that have become available recently and also drugs that are under trial for prophylaxis to prevent attacks. There is a paradigm shift to where the treatment of HAE is headed, focusing now on prophylactic treatment rather than abortive management. |
format | Online Article Text |
id | pubmed-5531155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-55311552017-08-04 Pediatric hereditary angioedema: an update Sabharwal, Geetika Craig, Timothy F1000Res Review Hereditary angioedema (HAE) with C1-inhibitor (C1-Inh) deficiency (C1-Inh-HAE) is a rare, life-threatening, and disabling genetic disorder characterized by self-limited tissue swelling caused by deficiency or dysfunction of C1-Inh. Our aim in this update is to discuss new advances in HAE therapy, focusing mainly on the various treatment options that have become available recently and also drugs that are under trial for prophylaxis to prevent attacks. There is a paradigm shift to where the treatment of HAE is headed, focusing now on prophylactic treatment rather than abortive management. F1000Research 2017-07-24 /pmc/articles/PMC5531155/ /pubmed/28781749 http://dx.doi.org/10.12688/f1000research.11320.1 Text en Copyright: © 2017 Sabharwal G and Craig T http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Sabharwal, Geetika Craig, Timothy Pediatric hereditary angioedema: an update |
title | Pediatric hereditary angioedema: an update |
title_full | Pediatric hereditary angioedema: an update |
title_fullStr | Pediatric hereditary angioedema: an update |
title_full_unstemmed | Pediatric hereditary angioedema: an update |
title_short | Pediatric hereditary angioedema: an update |
title_sort | pediatric hereditary angioedema: an update |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531155/ https://www.ncbi.nlm.nih.gov/pubmed/28781749 http://dx.doi.org/10.12688/f1000research.11320.1 |
work_keys_str_mv | AT sabharwalgeetika pediatrichereditaryangioedemaanupdate AT craigtimothy pediatrichereditaryangioedemaanupdate |