Neoplasias endócrinas múltiplas

Detalhes bibliográficos
Autor(a) principal: Guimarães, J
Data de Publicação: 2007
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.4/868
Resumo: The knowledge of genetics has increased in recent years and has led to important changes in management of hereditary diseases. Multiple endocrine neoplasia is characterized by the occurrence of benign or malign tumours involving two or more endocrine glands and two major forms are recognized: MEN1 and MEN2. All these forms of MEN are inherited as autosomal dominant syndromes. In this article we briefly review the clinic, diagnosis and treatment for the MEN1 and MEN2 and the indications for genetic testing.
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spelling Neoplasias endócrinas múltiplasMultiple endocrine neoplasiaNeoplasias Endócrinas MúltiplasThe knowledge of genetics has increased in recent years and has led to important changes in management of hereditary diseases. Multiple endocrine neoplasia is characterized by the occurrence of benign or malign tumours involving two or more endocrine glands and two major forms are recognized: MEN1 and MEN2. All these forms of MEN are inherited as autosomal dominant syndromes. In this article we briefly review the clinic, diagnosis and treatment for the MEN1 and MEN2 and the indications for genetic testing.RIHUCGuimarães, J2010-12-07T12:34:44Z20072007-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.4/868porActa Med Port. 2007 Jan-Feb;20(1):65-72.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-11T14:22:03Zoai:rihuc.huc.min-saude.pt:10400.4/868Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:03:24.517267Repositório 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 Neoplasias endócrinas múltiplas
Multiple endocrine neoplasia
title Neoplasias endócrinas múltiplas
spellingShingle Neoplasias endócrinas múltiplas
Guimarães, J
Neoplasias Endócrinas Múltiplas
title_short Neoplasias endócrinas múltiplas
title_full Neoplasias endócrinas múltiplas
title_fullStr Neoplasias endócrinas múltiplas
title_full_unstemmed Neoplasias endócrinas múltiplas
title_sort Neoplasias endócrinas múltiplas
author Guimarães, J
author_facet Guimarães, J
author_role author
dc.contributor.none.fl_str_mv RIHUC
dc.contributor.author.fl_str_mv Guimarães, J
dc.subject.por.fl_str_mv Neoplasias Endócrinas Múltiplas
topic Neoplasias Endócrinas Múltiplas
description The knowledge of genetics has increased in recent years and has led to important changes in management of hereditary diseases. Multiple endocrine neoplasia is characterized by the occurrence of benign or malign tumours involving two or more endocrine glands and two major forms are recognized: MEN1 and MEN2. All these forms of MEN are inherited as autosomal dominant syndromes. In this article we briefly review the clinic, diagnosis and treatment for the MEN1 and MEN2 and the indications for genetic testing.
publishDate 2007
dc.date.none.fl_str_mv 2007
2007-01-01T00:00:00Z
2010-12-07T12:34:44Z
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dc.language.iso.fl_str_mv por
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dc.relation.none.fl_str_mv Acta Med Port. 2007 Jan-Feb;20(1):65-72.
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