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DOI 10.1590/1678-4685-gmb-2018-0214

Медицинская библиотека · Genetics and molecular biology · 2019

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

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

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Аннотация

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.

Для цитирования: 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. Information and Diagnosis Networks - tools to improve diagnosis and treatment for patients with rare genetic diseases.. Genetics and molecular biology. 2019. DOI: 10.1590/1678-4685-gmb-2018-0214.
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