Syndrome in question
Autor(a) principal: | |
---|---|
Data de Publicação: | 2014 |
Outros Autores: | , , , , |
Tipo de documento: | Relatório |
Idioma: | eng |
Título da fonte: | Anais brasileiros de dermatologia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000601005 |
Resumo: | Costello syndrome (CS) is a rare genetic disorder, first described by Costello in 1971, caused by mutations in the HRAS proto-oncogene. Clinical findings include facial dysmorphism, skin disorders, cognitive impairment, cardiac and musculoskeletal defects. There is an increased risk of malignancies in these patients, due to the proto-oncogene mutation, and also sudden death secondary to heart disease. We report a case with characteristic phenotype, highlighting the peculiar skin changes. |
id |
SBD-1_61ff91f2ab55ae1531409bfaff045e41 |
---|---|
oai_identifier_str |
oai:scielo:S0365-05962014000601005 |
network_acronym_str |
SBD-1 |
network_name_str |
Anais brasileiros de dermatologia (Online) |
repository_id_str |
|
spelling |
Syndrome in questionCostello syndromeGenes, rasProto-oncogenesCostello syndrome (CS) is a rare genetic disorder, first described by Costello in 1971, caused by mutations in the HRAS proto-oncogene. Clinical findings include facial dysmorphism, skin disorders, cognitive impairment, cardiac and musculoskeletal defects. There is an increased risk of malignancies in these patients, due to the proto-oncogene mutation, and also sudden death secondary to heart disease. We report a case with characteristic phenotype, highlighting the peculiar skin changes.Sociedade Brasileira de Dermatologia2014-12-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000601005Anais Brasileiros de Dermatologia v.89 n.6 2014reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20143062info:eu-repo/semantics/openAccessPeixoto,Isy LimaCarreno,Ana MariaPrazeres,Vania Mesquita GadelhaChirano,Caroline Albuquerque RodriguesIhara,Gabriel MarojaAkel,Patricia Bandeira de Meloeng2015-03-25T00:00:00Zoai:scielo:S0365-05962014000601005Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2015-03-25T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false |
dc.title.none.fl_str_mv |
Syndrome in question |
title |
Syndrome in question |
spellingShingle |
Syndrome in question Peixoto,Isy Lima Costello syndrome Genes, ras Proto-oncogenes |
title_short |
Syndrome in question |
title_full |
Syndrome in question |
title_fullStr |
Syndrome in question |
title_full_unstemmed |
Syndrome in question |
title_sort |
Syndrome in question |
author |
Peixoto,Isy Lima |
author_facet |
Peixoto,Isy Lima Carreno,Ana Maria Prazeres,Vania Mesquita Gadelha Chirano,Caroline Albuquerque Rodrigues Ihara,Gabriel Maroja Akel,Patricia Bandeira de Melo |
author_role |
author |
author2 |
Carreno,Ana Maria Prazeres,Vania Mesquita Gadelha Chirano,Caroline Albuquerque Rodrigues Ihara,Gabriel Maroja Akel,Patricia Bandeira de Melo |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Peixoto,Isy Lima Carreno,Ana Maria Prazeres,Vania Mesquita Gadelha Chirano,Caroline Albuquerque Rodrigues Ihara,Gabriel Maroja Akel,Patricia Bandeira de Melo |
dc.subject.por.fl_str_mv |
Costello syndrome Genes, ras Proto-oncogenes |
topic |
Costello syndrome Genes, ras Proto-oncogenes |
description |
Costello syndrome (CS) is a rare genetic disorder, first described by Costello in 1971, caused by mutations in the HRAS proto-oncogene. Clinical findings include facial dysmorphism, skin disorders, cognitive impairment, cardiac and musculoskeletal defects. There is an increased risk of malignancies in these patients, due to the proto-oncogene mutation, and also sudden death secondary to heart disease. We report a case with characteristic phenotype, highlighting the peculiar skin changes. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-12-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/report |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
report |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000601005 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000601005 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/abd1806-4841.20143062 |
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.89 n.6 2014 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_ |
1752126420171096064 |