Information and Diagnosis Networks - tools to improve diagnosis and treatment for patients with rare genetic diseases

被引:0
|
作者
Vieira, Taiane Alves [1 ,2 ]
Trapp, Franciele Barbosa [1 ]
Moura de Souza, Carolina Fischinger [1 ]
Faccini, Lavinia Schuler [1 ,3 ]
Jardim, Laura Bannach [1 ,4 ]
Doederlein Schwartz, Ida Vanessa [1 ,3 ]
Riegel, Mariluce [1 ]
Vargas, Carmen Regla [1 ]
Burin, Maira Graeff [1 ]
Leistner-Segal, Sandra [1 ]
Ashton-Prolla, Patricia [1 ,2 ,3 ]
Giugliani, Roberto [1 ,3 ]
机构
[1] Hosp Clin Porto Alegre, Med Genet Serv, Rua Ramiro Barcelos 2350, BR-90035903 Porto Alegre, RS, Brazil
[2] Hosp Clin Porto Alegre, Res & Postgrad Grp, Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Dept Genet, Porto Alegre, RS, Brazil
[4] Univ Fed Rio Grande do Sul, Dept Internal Med, Porto Alegre, RS, Brazil
关键词
Information services; Medical Genetics; diagnostic networks; rare diseases; reference centers; MITOCHONDRIAL POLYMORPHISM A10398G; BRAZIL; HAPLOTYPE; ATAXIAS; WOMEN;
D O I
10.1590/1678-4685-GMB-2018-0214
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 Clinicas 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), Alo Genetica (Hello Genetics - Medical Genetics Information Service for Primary Health Care Professionals); Rede MPS Brasil (MPS-Mucopolysaccharidosis Brazil Network); Rede EIM Brasil (I EM-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 Neurogenetica (Neurogenetics Network), and Rede Brasileira de Cancer Hereditario (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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页码:155 / 164
页数:10
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