XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?.
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/888 |
Resumo: | The XYY male has characteristicaly tall stature, behavior problems and speech delay. There may may be an association with nephro-urologic malformations but cardiovascular anomalies are usually not present.It is reported a case of a boy with a 47 XYY karyotype with persistent respiratory distress and swallowing difficulties since two months old. On diagnosis workup the fiberoptic bronchoscopy showed a significant pulsatil tracheal obstruction at its right lateral wall and the magnetic resonance imaging of the mediastinum comproved the presence of a vascular ring (right aortic arch with left ligamentum arteriosum). The patient was submitted to surgery with improvment in the respiratory symptoms.The XYY male is a sex chromosomal abnormality that usually is not associated with cardiovascular malformations. A vascular ring presents with persistent respiratory distress and feeding difficulties; the begining and severity of the symptoms varies with the type of vascular ring. The main procedure to be requested is the fiberoptic bronchoscopy and the best image study is the magnetic resonance imaging of the mediastinum. |
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XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?.Síndroma 47 XYY com arco aórtico direito e ligamentum arteriosum: uma associação fortuita?The XYY male has characteristicaly tall stature, behavior problems and speech delay. There may may be an association with nephro-urologic malformations but cardiovascular anomalies are usually not present.It is reported a case of a boy with a 47 XYY karyotype with persistent respiratory distress and swallowing difficulties since two months old. On diagnosis workup the fiberoptic bronchoscopy showed a significant pulsatil tracheal obstruction at its right lateral wall and the magnetic resonance imaging of the mediastinum comproved the presence of a vascular ring (right aortic arch with left ligamentum arteriosum). The patient was submitted to surgery with improvment in the respiratory symptoms.The XYY male is a sex chromosomal abnormality that usually is not associated with cardiovascular malformations. A vascular ring presents with persistent respiratory distress and feeding difficulties; the begining and severity of the symptoms varies with the type of vascular ring. The main procedure to be requested is the fiberoptic bronchoscopy and the best image study is the magnetic resonance imaging of the mediastinum.The XYY male has characteristicaly tall stature, behavior problems and speech delay. There may may be an association with nephro-urologic malformations but cardiovascular anomalies are usually not present.It is reported a case of a boy with a 47 XYY karyotype with persistent respiratory distress and swallowing difficulties since two months old. On diagnosis workup the fiberoptic bronchoscopy showed a significant pulsatil tracheal obstruction at its right lateral wall and the magnetic resonance imaging of the mediastinum comproved the presence of a vascular ring (right aortic arch with left ligamentum arteriosum). The patient was submitted to surgery with improvment in the respiratory symptoms.The XYY male is a sex chromosomal abnormality that usually is not associated with cardiovascular malformations. A vascular ring presents with persistent respiratory distress and feeding difficulties; the begining and severity of the symptoms varies with the type of vascular ring. The main procedure to be requested is the fiberoptic bronchoscopy and the best image study is the magnetic resonance imaging of the mediastinum.Ordem dos Médicos2008-02-13info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/888oai:ojs.www.actamedicaportuguesa.com:article/888Acta Médica Portuguesa; Vol. 20 No. 6 (2007): November-December; 575-80Acta Médica Portuguesa; Vol. 20 N.º 6 (2007): Novembro-Dezembro; 575-801646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/888https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/888/562Amador, AntónioMartins, IsabelMassa, RosárioOliveira Santos, Jinfo:eu-repo/semantics/openAccess2022-12-20T10:57:07Zoai:ojs.www.actamedicaportuguesa.com:article/888Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:16:49.893408Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?. Síndroma 47 XYY com arco aórtico direito e ligamentum arteriosum: uma associação fortuita? |
title |
XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?. |
spellingShingle |
XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?. Amador, António |
title_short |
XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?. |
title_full |
XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?. |
title_fullStr |
XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?. |
title_full_unstemmed |
XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?. |
title_sort |
XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?. |
author |
Amador, António |
author_facet |
Amador, António Martins, Isabel Massa, Rosário Oliveira Santos, J |
author_role |
author |
author2 |
Martins, Isabel Massa, Rosário Oliveira Santos, J |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Amador, António Martins, Isabel Massa, Rosário Oliveira Santos, J |
description |
The XYY male has characteristicaly tall stature, behavior problems and speech delay. There may may be an association with nephro-urologic malformations but cardiovascular anomalies are usually not present.It is reported a case of a boy with a 47 XYY karyotype with persistent respiratory distress and swallowing difficulties since two months old. On diagnosis workup the fiberoptic bronchoscopy showed a significant pulsatil tracheal obstruction at its right lateral wall and the magnetic resonance imaging of the mediastinum comproved the presence of a vascular ring (right aortic arch with left ligamentum arteriosum). The patient was submitted to surgery with improvment in the respiratory symptoms.The XYY male is a sex chromosomal abnormality that usually is not associated with cardiovascular malformations. A vascular ring presents with persistent respiratory distress and feeding difficulties; the begining and severity of the symptoms varies with the type of vascular ring. The main procedure to be requested is the fiberoptic bronchoscopy and the best image study is the magnetic resonance imaging of the mediastinum. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-02-13 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/888 oai:ojs.www.actamedicaportuguesa.com:article/888 |
url |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/888 |
identifier_str_mv |
oai:ojs.www.actamedicaportuguesa.com:article/888 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/888 https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/888/562 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Ordem dos Médicos |
publisher.none.fl_str_mv |
Ordem dos Médicos |
dc.source.none.fl_str_mv |
Acta Médica Portuguesa; Vol. 20 No. 6 (2007): November-December; 575-80 Acta Médica Portuguesa; Vol. 20 N.º 6 (2007): Novembro-Dezembro; 575-80 1646-0758 0870-399X reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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