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Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases

Epidermolysis bullosa (EB) comprises a group of genetic disorders with the hallmark of fragility of the skin and mucosal surfaces. The severity of different types of EB varies markedly as does the occurrence of extra-cutaneous involvement and complications. A number of emergency situations may occur...

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Autores principales: Mellerio, Jemima E., El Hachem, Maya, Bellon, Nathalia, Zambruno, Giovanna, Buckova, Hana, Autrata, Rudolf, Salavastru, Carmen, Caldaro, Tamara, Greco, Celine, Has, Cristina, Bodemer, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276067/
https://www.ncbi.nlm.nih.gov/pubmed/32505191
http://dx.doi.org/10.1186/s13023-020-01403-x
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author Mellerio, Jemima E.
El Hachem, Maya
Bellon, Nathalia
Zambruno, Giovanna
Buckova, Hana
Autrata, Rudolf
Salavastru, Carmen
Caldaro, Tamara
Greco, Celine
Has, Cristina
Bodemer, Christine
author_facet Mellerio, Jemima E.
El Hachem, Maya
Bellon, Nathalia
Zambruno, Giovanna
Buckova, Hana
Autrata, Rudolf
Salavastru, Carmen
Caldaro, Tamara
Greco, Celine
Has, Cristina
Bodemer, Christine
author_sort Mellerio, Jemima E.
collection PubMed
description Epidermolysis bullosa (EB) comprises a group of genetic disorders with the hallmark of fragility of the skin and mucosal surfaces. The severity of different types of EB varies markedly as does the occurrence of extra-cutaneous involvement and complications. A number of emergency situations may occur in the context of EB including obstruction to oral intake from oral or esophageal blisters or scarring, acute airway obstruction, acute urinary retention, sepsis and corneal erosions. Whilst general management principles apply in each of these settings, specific considerations are essential in managing EB to avoid undue trauma or damage to delicate tissues. These recommendations have been developed from a literature review and consensus from experts of the European Network for Rare Skin Disorders (ERN-Skin) to aid decision-making and optimize clinical care by non-EB expert health professionals encountering emergency situations in babies, children and adults with EB.
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spelling pubmed-72760672020-06-08 Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases Mellerio, Jemima E. El Hachem, Maya Bellon, Nathalia Zambruno, Giovanna Buckova, Hana Autrata, Rudolf Salavastru, Carmen Caldaro, Tamara Greco, Celine Has, Cristina Bodemer, Christine Orphanet J Rare Dis Review Epidermolysis bullosa (EB) comprises a group of genetic disorders with the hallmark of fragility of the skin and mucosal surfaces. The severity of different types of EB varies markedly as does the occurrence of extra-cutaneous involvement and complications. A number of emergency situations may occur in the context of EB including obstruction to oral intake from oral or esophageal blisters or scarring, acute airway obstruction, acute urinary retention, sepsis and corneal erosions. Whilst general management principles apply in each of these settings, specific considerations are essential in managing EB to avoid undue trauma or damage to delicate tissues. These recommendations have been developed from a literature review and consensus from experts of the European Network for Rare Skin Disorders (ERN-Skin) to aid decision-making and optimize clinical care by non-EB expert health professionals encountering emergency situations in babies, children and adults with EB. BioMed Central 2020-06-06 /pmc/articles/PMC7276067/ /pubmed/32505191 http://dx.doi.org/10.1186/s13023-020-01403-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Mellerio, Jemima E.
El Hachem, Maya
Bellon, Nathalia
Zambruno, Giovanna
Buckova, Hana
Autrata, Rudolf
Salavastru, Carmen
Caldaro, Tamara
Greco, Celine
Has, Cristina
Bodemer, Christine
Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases
title Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases
title_full Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases
title_fullStr Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases
title_full_unstemmed Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases
title_short Emergency management in epidermolysis bullosa: consensus clinical recommendations from the European reference network for rare skin diseases
title_sort emergency management in epidermolysis bullosa: consensus clinical recommendations from the european reference network for rare skin diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276067/
https://www.ncbi.nlm.nih.gov/pubmed/32505191
http://dx.doi.org/10.1186/s13023-020-01403-x
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