Information and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseases

Detalhes bibliográficos
Autor(a) principal: Vieira, Taiane Alves
Data de Publicação: 2019
Outros Autores: Trapp, Franciele Barbosa, Souza, Carolina Fischinger Moura de, Faccini, Lavinia Schuler, Jardim, Laura Bannach, Schwartz, Ida Vanessa Doederlein, Riegel, Mariluce, Vargas, Carmen Regla, Burin, Maira Graeff, Leistner-Segal, Sandra, Prolla, Patrícia Ashton, Giugliani, Roberto
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/201010
Resumo: Brazil is a country of continental dimensions and most genetic services are concentrated in the Southeast and South, including the Medical Genetics Service of the Hospital de Clínicas de Porto Alegre (MGS/HCPA). As many areas on the country do not have adequate medical genetics support, networks were designed to extend the service of the MGS/HCPA reference center. This paper presents the information and diagnosis networks that have their headquarters at MGS/HCPA: SIAT (National Information System on Teratogenic Agents), SIEM (Information Service on Inborn Errors of Metabolism), Alô Genética (Hello Genetics - Medical Genetics Information Service for Primary Health Care Professionals); Rede MPS Brasil (MPS-Mucopolysaccharidosis Brazil Network); Rede EIM Brasil (IEM-Inborn Errors of Metabolism Brazil Network), Rede NPC Brasil (Niemann-Pick C - NPC Brazil Network), Rede DLD Brasil (LSD-Lysosomal Storage Disorders Brazil Network), Rede DXB (MSUD-Maple Syrup Urine Disease Network), RedeBRIM (Brazilian Network of Reference and Information in Microdeletion Syndromes Project), Rede Neurogenética (Neurogenetics Network), and Rede Brasileira de Câncer Hereditário (Brazilian Hereditary Cancer Network). These tools are very useful to provide access to a qualified information and/or diagnostic service for specialized and non-specialized health services, bypassing difficulties that preclude patients to access reference centers.
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spelling Vieira, Taiane AlvesTrapp, Franciele BarbosaSouza, Carolina Fischinger Moura deFaccini, Lavinia SchulerJardim, Laura BannachSchwartz, Ida Vanessa DoederleinRiegel, MariluceVargas, Carmen ReglaBurin, Maira GraeffLeistner-Segal, SandraProlla, Patrícia AshtonGiugliani, Roberto2019-10-25T03:47:05Z20191415-4757http://hdl.handle.net/10183/201010001099527Brazil is a country of continental dimensions and most genetic services are concentrated in the Southeast and South, including the Medical Genetics Service of the Hospital de Clínicas de Porto Alegre (MGS/HCPA). As many areas on the country do not have adequate medical genetics support, networks were designed to extend the service of the MGS/HCPA reference center. This paper presents the information and diagnosis networks that have their headquarters at MGS/HCPA: SIAT (National Information System on Teratogenic Agents), SIEM (Information Service on Inborn Errors of Metabolism), Alô Genética (Hello Genetics - Medical Genetics Information Service for Primary Health Care Professionals); Rede MPS Brasil (MPS-Mucopolysaccharidosis Brazil Network); Rede EIM Brasil (IEM-Inborn Errors of Metabolism Brazil Network), Rede NPC Brasil (Niemann-Pick C - NPC Brazil Network), Rede DLD Brasil (LSD-Lysosomal Storage Disorders Brazil Network), Rede DXB (MSUD-Maple Syrup Urine Disease Network), RedeBRIM (Brazilian Network of Reference and Information in Microdeletion Syndromes Project), Rede Neurogenética (Neurogenetics Network), and Rede Brasileira de Câncer Hereditário (Brazilian Hereditary Cancer Network). These tools are very useful to provide access to a qualified information and/or diagnostic service for specialized and non-specialized health services, bypassing difficulties that preclude patients to access reference centers.application/pdfengGenetics and molecular biology. Ribeirão Preto. Vol. 42, no. 1 suppl. 1 (2019), p. 155-164Doenças genéticas inatasServiços de informaçãoInformation servicesMedical geneticsDiagnostic networksRare diseasesReference centersInformation and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseasesinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001099527.pdf.txt001099527.pdf.txtExtracted Texttext/plain48048http://www.lume.ufrgs.br/bitstream/10183/201010/2/001099527.pdf.txt73d9b85721ca2eb52c9d713e109d63a0MD52ORIGINAL001099527.pdfTexto completo (inglês)application/pdf1248813http://www.lume.ufrgs.br/bitstream/10183/201010/1/001099527.pdfd1fb2e981a6539d1500e66dcb0f5ed0eMD5110183/2010102022-12-07 05:51:51.335766oai:www.lume.ufrgs.br:10183/201010Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2022-12-07T07:51:51Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Information and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseases
title Information and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseases
spellingShingle Information and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseases
Vieira, Taiane Alves
Doenças genéticas inatas
Serviços de informação
Information services
Medical genetics
Diagnostic networks
Rare diseases
Reference centers
title_short Information and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseases
title_full Information and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseases
title_fullStr Information and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseases
title_full_unstemmed Information and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseases
title_sort Information and diagnosis networks : tools to improve diagnosis and treatment for patients with rare genetic diseases
author Vieira, Taiane Alves
author_facet Vieira, Taiane Alves
Trapp, Franciele Barbosa
Souza, Carolina Fischinger Moura de
Faccini, Lavinia Schuler
Jardim, Laura Bannach
Schwartz, Ida Vanessa Doederlein
Riegel, Mariluce
Vargas, Carmen Regla
Burin, Maira Graeff
Leistner-Segal, Sandra
Prolla, Patrícia Ashton
Giugliani, Roberto
author_role author
author2 Trapp, Franciele Barbosa
Souza, Carolina Fischinger Moura de
Faccini, Lavinia Schuler
Jardim, Laura Bannach
Schwartz, Ida Vanessa Doederlein
Riegel, Mariluce
Vargas, Carmen Regla
Burin, Maira Graeff
Leistner-Segal, Sandra
Prolla, Patrícia Ashton
Giugliani, Roberto
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Vieira, Taiane Alves
Trapp, Franciele Barbosa
Souza, Carolina Fischinger Moura de
Faccini, Lavinia Schuler
Jardim, Laura Bannach
Schwartz, Ida Vanessa Doederlein
Riegel, Mariluce
Vargas, Carmen Regla
Burin, Maira Graeff
Leistner-Segal, Sandra
Prolla, Patrícia Ashton
Giugliani, Roberto
dc.subject.por.fl_str_mv Doenças genéticas inatas
Serviços de informação
topic Doenças genéticas inatas
Serviços de informação
Information services
Medical genetics
Diagnostic networks
Rare diseases
Reference centers
dc.subject.eng.fl_str_mv Information services
Medical genetics
Diagnostic networks
Rare diseases
Reference centers
description Brazil is a country of continental dimensions and most genetic services are concentrated in the Southeast and South, including the Medical Genetics Service of the Hospital de Clínicas de Porto Alegre (MGS/HCPA). As many areas on the country do not have adequate medical genetics support, networks were designed to extend the service of the MGS/HCPA reference center. This paper presents the information and diagnosis networks that have their headquarters at MGS/HCPA: SIAT (National Information System on Teratogenic Agents), SIEM (Information Service on Inborn Errors of Metabolism), Alô Genética (Hello Genetics - Medical Genetics Information Service for Primary Health Care Professionals); Rede MPS Brasil (MPS-Mucopolysaccharidosis Brazil Network); Rede EIM Brasil (IEM-Inborn Errors of Metabolism Brazil Network), Rede NPC Brasil (Niemann-Pick C - NPC Brazil Network), Rede DLD Brasil (LSD-Lysosomal Storage Disorders Brazil Network), Rede DXB (MSUD-Maple Syrup Urine Disease Network), RedeBRIM (Brazilian Network of Reference and Information in Microdeletion Syndromes Project), Rede Neurogenética (Neurogenetics Network), and Rede Brasileira de Câncer Hereditário (Brazilian Hereditary Cancer Network). These tools are very useful to provide access to a qualified information and/or diagnostic service for specialized and non-specialized health services, bypassing difficulties that preclude patients to access reference centers.
publishDate 2019
dc.date.accessioned.fl_str_mv 2019-10-25T03:47:05Z
dc.date.issued.fl_str_mv 2019
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/201010
dc.identifier.issn.pt_BR.fl_str_mv 1415-4757
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Genetics and molecular biology. Ribeirão Preto. Vol. 42, no. 1 suppl. 1 (2019), p. 155-164
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
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