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,Lavínia Schuler, Jardim,Laura Bannach, Schwartz,Ida Vanessa Doederlein, Riegel,Mariluce, Vargas,Carmen Regla, Burin,Maira Graeff, Leistner-Segal,Sandra, Ashton-Prolla,Patrícia, Giugliani,Roberto
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Genetics and Molecular Biology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019000200155
Resumo: Abstract 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 Information and Diagnosis Networks – tools to improve diagnosis and treatment for patients with rare genetic diseasesInformation servicesMedical Geneticsdiagnostic networksrare diseasesreference centersAbstract 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.Sociedade Brasileira de Genética2019-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019000200155Genetics and Molecular Biology v.42 n.1 suppl.1 2019reponame:Genetics and Molecular Biologyinstname:Sociedade Brasileira de Genética (SBG)instacron:SBG10.1590/1678-4685-gmb-2018-0214info:eu-repo/semantics/openAccessVieira,Taiane AlvesTrapp,Franciele BarbosaSouza,Carolina Fischinger Moura deFaccini,Lavínia SchulerJardim,Laura BannachSchwartz,Ida Vanessa DoederleinRiegel,MariluceVargas,Carmen ReglaBurin,Maira GraeffLeistner-Segal,SandraAshton-Prolla,PatríciaGiugliani,Robertoeng2019-07-12T00:00:00Zoai:scielo:S1415-47572019000200155Revistahttp://www.gmb.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||editor@gmb.org.br1678-46851415-4757opendoar:2019-07-12T00:00Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)false
dc.title.none.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
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,Lavínia Schuler
Jardim,Laura Bannach
Schwartz,Ida Vanessa Doederlein
Riegel,Mariluce
Vargas,Carmen Regla
Burin,Maira Graeff
Leistner-Segal,Sandra
Ashton-Prolla,Patrícia
Giugliani,Roberto
author_role author
author2 Trapp,Franciele Barbosa
Souza,Carolina Fischinger Moura de
Faccini,Lavínia Schuler
Jardim,Laura Bannach
Schwartz,Ida Vanessa Doederlein
Riegel,Mariluce
Vargas,Carmen Regla
Burin,Maira Graeff
Leistner-Segal,Sandra
Ashton-Prolla,Patrícia
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,Lavínia Schuler
Jardim,Laura Bannach
Schwartz,Ida Vanessa Doederlein
Riegel,Mariluce
Vargas,Carmen Regla
Burin,Maira Graeff
Leistner-Segal,Sandra
Ashton-Prolla,Patrícia
Giugliani,Roberto
dc.subject.por.fl_str_mv Information services
Medical Genetics
diagnostic networks
rare diseases
reference centers
topic Information services
Medical Genetics
diagnostic networks
rare diseases
reference centers
description Abstract 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.none.fl_str_mv 2019-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019000200155
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019000200155
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1678-4685-gmb-2018-0214
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 Genética
publisher.none.fl_str_mv Sociedade Brasileira de Genética
dc.source.none.fl_str_mv Genetics and Molecular Biology v.42 n.1 suppl.1 2019
reponame:Genetics and Molecular Biology
instname:Sociedade Brasileira de Genética (SBG)
instacron:SBG
instname_str Sociedade Brasileira de Genética (SBG)
instacron_str SBG
institution SBG
reponame_str Genetics and Molecular Biology
collection Genetics and Molecular Biology
repository.name.fl_str_mv Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)
repository.mail.fl_str_mv ||editor@gmb.org.br
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