{"id":4821,"date":"2019-11-13T09:33:08","date_gmt":"2019-11-13T09:33:08","guid":{"rendered":"https:\/\/sindromecharge.es\/index.php\/2019\/11\/13\/feder-en-la-iii-jornada-del-genoma-humano-patrimonio-de-la-humanidad\/"},"modified":"2019-11-13T09:33:08","modified_gmt":"2019-11-13T09:33:08","slug":"feder-en-la-iii-jornada-del-genoma-humano-patrimonio-de-la-humanidad","status":"publish","type":"post","link":"https:\/\/sindromecharge.es\/index.php\/2019\/11\/13\/feder-en-la-iii-jornada-del-genoma-humano-patrimonio-de-la-humanidad\/","title":{"rendered":"FEDER en la III Jornada del Genoma Humano Patrimonio de la Humanidad"},"content":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: <\/p>\n<p>&nbsp;<\/p>\n<p>El Hospital Universitario Ram\u00f3n y Cajal de Madrid organiza el 13 de noviembre la III Jornada del Genoma Humano Patrimonio de la Humanidad que en esta ocasi\u00f3n ir\u00e1 dedicada a \u2018La medicina gen\u00f3mica personalizada y aproximaciones terape\u00faticas en ER\u2019.<\/p>\n<p>Desde FEDER hemos querido estar presente en este evento y por ello estaremos representados por nuestro Tesorero y Vicepresidente de nuestra Fundaci\u00f3n, Santiago de la Riva, quien participar\u00e1 en un taller que abordar\u00e1 la medicina de precisi\u00f3n en las Enfermedades Raras y donde se debatir\u00e1 sobre el papel central que debe jugar los pacientes, el genetista y el especialista cl\u00ednico.<\/p>\n<p>Enmarcado en el 22\u00ba aniversario de la declaraci\u00f3n del Genoma Humano como Patrimonio de la Humanidad, se celebra esta jornada donde podr\u00e1 conocer m\u00e1s de cerca los avances en las aplicaciones de la Next Generation Sequencing NGS en el \u00e1mbito cl\u00ednico y de investigaci\u00f3n traslacional (diagn\u00f3stico prenatal, caracterizaci\u00f3n molecular de tumores, edici\u00f3n gen\u00f3mica, etc.), las iniciativas de integraci\u00f3n de los estudios gen\u00f3micos de la red hospitalaria (Proyecto CMAG del SERMAS, Red Raregenomics de la Comunidad de Madrid), el uso de la inteligencia artificial y el BIG DATA cl\u00ednico para el correcto desarrollo de la Medicina Gen\u00f3mica Personalizada en enfermedades raras y su implantaci\u00f3n en el Sistema Nacional de Salud. Tambi\u00e9n se mostrar\u00e1n los avances que se est\u00e1n logrando en el desarrollo de abordajes terap\u00e9uticos en distintas enfermedades raras.<\/p>\n<p><span style=\"font-size: 12pt\">\u00bfQu\u00e9 es la Next Generation Sequencing?<\/span><\/p>\n<p>Es una herramienta de diagn\u00f3stico gen\u00e9tico consolidada en la pr\u00e1ctica cl\u00ednica que tiene un especial impacto en el diagn\u00f3stico y en el desarrollo.<\/p>\n<p><span style=\"font-size: 12pt\">El conocimiento, fundamental para las Enfermedades Raras<\/span><\/p>\n<p>Gracias a estos eventos se consigue impulsar el conocimiento, aspecto fundamental para obtener un correcto abordaje de las enfermedades raras y que a trav\u00e9s de \u00e9l, los pacientes y familiares tendr\u00e1n una mejor calidad de vida.<\/p>\n<p>&nbsp;<\/p>\n<p>Fuente: FEDER <a href=\"https:\/\/enfermedades-raras.org\/index.php\/actualidad\/noticias-eventos\/2-feder\/13217-feder-en-la-iii-jornada-del-genoma-humano-patrimonio-de-la-humanidad\" target=\"_blank\" rel=\"noopener noreferrer\">FEDER en la III Jornada del Genoma Humano Patrimonio de la Humanidad<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: &nbsp; El Hospital Universitario Ram\u00f3n y Cajal de Madrid organiza el 13 de noviembre la III Jornada del Genoma Humano Patrimonio de la Humanidad que en esta ocasi\u00f3n ir\u00e1 dedicada a \u2018La medicina gen\u00f3mica personalizada y aproximaciones terape\u00faticas en ER\u2019. Desde FEDER hemos [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[8],"tags":[36],"class_list":["post-4821","post","type-post","status-publish","format-standard","hentry","category-noticias","tag-enfermedades-raras"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>FEDER en la III Jornada del Genoma Humano Patrimonio de la Humanidad - Asociaci\u00f3n Espa\u00f1ola S\u00edndrome de Charge<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/sindromecharge.es\/index.php\/2019\/11\/13\/feder-en-la-iii-jornada-del-genoma-humano-patrimonio-de-la-humanidad\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"FEDER en la III Jornada del Genoma Humano Patrimonio de la Humanidad - Asociaci\u00f3n Espa\u00f1ola S\u00edndrome de Charge\" \/>\n<meta property=\"og:description\" content=\"Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: &nbsp; El Hospital Universitario Ram\u00f3n y Cajal de Madrid organiza el 13 de noviembre la III Jornada del Genoma Humano Patrimonio de la Humanidad que en esta ocasi\u00f3n ir\u00e1 dedicada a \u2018La medicina gen\u00f3mica personalizada y aproximaciones terape\u00faticas en ER\u2019. 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