Von Recklinghausen's neurofibromatosis.

Detalhes bibliográficos
Autor(a) principal: Ventura, A
Data de Publicação: 1989
Outros Autores: Murinello, A, Ribeiro, J, Morgado, A, Mota, J A
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/3477
Resumo: Neurofibromatosis is a multisystemic disease in which the multiple possible clinical manifestations may have important diagnostic and prognostic implications; if arterial hypertension coexists, many pathogenic mechanisms justify that the possible secondary etiology must be considered. In this report we review the pathogenic and clinical mechanisms and we point to the diagnostic strategy to reveal anomalies and diseases that, although present, may be occult.
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spelling Von Recklinghausen's neurofibromatosis.Neurofibromatose de von Recklinghausen.Neurofibromatosis is a multisystemic disease in which the multiple possible clinical manifestations may have important diagnostic and prognostic implications; if arterial hypertension coexists, many pathogenic mechanisms justify that the possible secondary etiology must be considered. In this report we review the pathogenic and clinical mechanisms and we point to the diagnostic strategy to reveal anomalies and diseases that, although present, may be occult.Neurofibromatosis is a multisystemic disease in which the multiple possible clinical manifestations may have important diagnostic and prognostic implications; if arterial hypertension coexists, many pathogenic mechanisms justify that the possible secondary etiology must be considered. In this report we review the pathogenic and clinical mechanisms and we point to the diagnostic strategy to reveal anomalies and diseases that, although present, may be occult.Ordem dos Médicos1989-06-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3477oai:ojs.www.actamedicaportuguesa.com:article/3477Acta Médica Portuguesa; Vol. 2 No. 3 (1989): Maio-Junho; 163-6Acta Médica Portuguesa; Vol. 2 N.º 3 (1989): Maio-Junho; 163-61646-07580870-399Xreponame: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/3477https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3477/2767Ventura, AMurinello, ARibeiro, JMorgado, AMota, J Ainfo:eu-repo/semantics/openAccess2022-12-20T11:02:14Zoai:ojs.www.actamedicaportuguesa.com:article/3477Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:18:22.375589Repositório 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 Von Recklinghausen's neurofibromatosis.
Neurofibromatose de von Recklinghausen.
title Von Recklinghausen's neurofibromatosis.
spellingShingle Von Recklinghausen's neurofibromatosis.
Ventura, A
title_short Von Recklinghausen's neurofibromatosis.
title_full Von Recklinghausen's neurofibromatosis.
title_fullStr Von Recklinghausen's neurofibromatosis.
title_full_unstemmed Von Recklinghausen's neurofibromatosis.
title_sort Von Recklinghausen's neurofibromatosis.
author Ventura, A
author_facet Ventura, A
Murinello, A
Ribeiro, J
Morgado, A
Mota, J A
author_role author
author2 Murinello, A
Ribeiro, J
Morgado, A
Mota, J A
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Ventura, A
Murinello, A
Ribeiro, J
Morgado, A
Mota, J A
description Neurofibromatosis is a multisystemic disease in which the multiple possible clinical manifestations may have important diagnostic and prognostic implications; if arterial hypertension coexists, many pathogenic mechanisms justify that the possible secondary etiology must be considered. In this report we review the pathogenic and clinical mechanisms and we point to the diagnostic strategy to reveal anomalies and diseases that, although present, may be occult.
publishDate 1989
dc.date.none.fl_str_mv 1989-06-30
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3477
oai:ojs.www.actamedicaportuguesa.com:article/3477
url https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3477
identifier_str_mv oai:ojs.www.actamedicaportuguesa.com:article/3477
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/3477
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/3477/2767
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. 2 No. 3 (1989): Maio-Junho; 163-6
Acta Médica Portuguesa; Vol. 2 N.º 3 (1989): Maio-Junho; 163-6
1646-0758
0870-399X
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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instacron_str RCAAP
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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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