Inherited epidermolysis bullosa: clinical and therapeutic aspects
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Anais brasileiros de dermatologia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000200185 |
Resumo: | Inherited epidermolysis bullosa (EB) is a heterogeneous group of genetic disorders that present with skin and, in some cases, mucosal fragility, predisposing patients to the development of blisters and/or erosions after minimal trauma or friction. Children with a recurrent history of these kinds of lesions or neonates that present them in the absence of another reasonable explanation should be investigated. Diagnosis must be based on clinical and histopathological findings. To date, management of inherited EB basically consists in avoiding traumas that trigger lesions, as well as preventing infection and facilitating healing of the wounds with the systematic use of bandages. |
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Anais brasileiros de dermatologia (Online) |
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Inherited epidermolysis bullosa: clinical and therapeutic aspectsEpidermolysis bullosaEpidermolysis bullosa dystrophicaEpidermolysis bullosa, junctionalEpidermolysis bullosa simplexInherited epidermolysis bullosa (EB) is a heterogeneous group of genetic disorders that present with skin and, in some cases, mucosal fragility, predisposing patients to the development of blisters and/or erosions after minimal trauma or friction. Children with a recurrent history of these kinds of lesions or neonates that present them in the absence of another reasonable explanation should be investigated. Diagnosis must be based on clinical and histopathological findings. To date, management of inherited EB basically consists in avoiding traumas that trigger lesions, as well as preventing infection and facilitating healing of the wounds with the systematic use of bandages.Sociedade Brasileira de Dermatologia2013-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000200185Anais Brasileiros de Dermatologia v.88 n.2 2013reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/S0365-05962013000200001info:eu-repo/semantics/openAccessBoeira,Vanessa Lys Simas YamakawaSouza,Erica SalesRocha,Bruno de OliveiraOliveira,Pedro DantasOliveira,Maria de Fátima Santos Paim deRêgo,Vitória Regina Pedreira de AlmeidaFollador,Ivoniseeng2013-06-04T00:00:00Zoai:scielo:S0365-05962013000200185Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2013-06-04T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false |
dc.title.none.fl_str_mv |
Inherited epidermolysis bullosa: clinical and therapeutic aspects |
title |
Inherited epidermolysis bullosa: clinical and therapeutic aspects |
spellingShingle |
Inherited epidermolysis bullosa: clinical and therapeutic aspects Boeira,Vanessa Lys Simas Yamakawa Epidermolysis bullosa Epidermolysis bullosa dystrophica Epidermolysis bullosa, junctional Epidermolysis bullosa simplex |
title_short |
Inherited epidermolysis bullosa: clinical and therapeutic aspects |
title_full |
Inherited epidermolysis bullosa: clinical and therapeutic aspects |
title_fullStr |
Inherited epidermolysis bullosa: clinical and therapeutic aspects |
title_full_unstemmed |
Inherited epidermolysis bullosa: clinical and therapeutic aspects |
title_sort |
Inherited epidermolysis bullosa: clinical and therapeutic aspects |
author |
Boeira,Vanessa Lys Simas Yamakawa |
author_facet |
Boeira,Vanessa Lys Simas Yamakawa Souza,Erica Sales Rocha,Bruno de Oliveira Oliveira,Pedro Dantas Oliveira,Maria de Fátima Santos Paim de Rêgo,Vitória Regina Pedreira de Almeida Follador,Ivonise |
author_role |
author |
author2 |
Souza,Erica Sales Rocha,Bruno de Oliveira Oliveira,Pedro Dantas Oliveira,Maria de Fátima Santos Paim de Rêgo,Vitória Regina Pedreira de Almeida Follador,Ivonise |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Boeira,Vanessa Lys Simas Yamakawa Souza,Erica Sales Rocha,Bruno de Oliveira Oliveira,Pedro Dantas Oliveira,Maria de Fátima Santos Paim de Rêgo,Vitória Regina Pedreira de Almeida Follador,Ivonise |
dc.subject.por.fl_str_mv |
Epidermolysis bullosa Epidermolysis bullosa dystrophica Epidermolysis bullosa, junctional Epidermolysis bullosa simplex |
topic |
Epidermolysis bullosa Epidermolysis bullosa dystrophica Epidermolysis bullosa, junctional Epidermolysis bullosa simplex |
description |
Inherited epidermolysis bullosa (EB) is a heterogeneous group of genetic disorders that present with skin and, in some cases, mucosal fragility, predisposing patients to the development of blisters and/or erosions after minimal trauma or friction. Children with a recurrent history of these kinds of lesions or neonates that present them in the absence of another reasonable explanation should be investigated. Diagnosis must be based on clinical and histopathological findings. To date, management of inherited EB basically consists in avoiding traumas that trigger lesions, as well as preventing infection and facilitating healing of the wounds with the systematic use of bandages. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-04-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000200185 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000200185 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0365-05962013000200001 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Dermatologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Dermatologia |
dc.source.none.fl_str_mv |
Anais Brasileiros de Dermatologia v.88 n.2 2013 reponame:Anais brasileiros de dermatologia (Online) instname:Sociedade Brasileira de Dermatologia (SBD) instacron:SBD |
instname_str |
Sociedade Brasileira de Dermatologia (SBD) |
instacron_str |
SBD |
institution |
SBD |
reponame_str |
Anais brasileiros de dermatologia (Online) |
collection |
Anais brasileiros de dermatologia (Online) |
repository.name.fl_str_mv |
Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD) |
repository.mail.fl_str_mv |
abd@sbd.org.br||revista@sbd.org.br |
_version_ |
1752126418617106432 |