{"id":4749,"date":"2019-10-25T07:31:43","date_gmt":"2019-10-25T07:31:43","guid":{"rendered":"https:\/\/sindromecharge.es\/index.php\/2019\/10\/25\/participamos-en-el-xiv-congreso-nacional-del-sindrome-de-cornelia-de-lange\/"},"modified":"2019-10-25T07:31:43","modified_gmt":"2019-10-25T07:31:43","slug":"participamos-en-el-xiv-congreso-nacional-del-sindrome-de-cornelia-de-lange","status":"publish","type":"post","link":"https:\/\/sindromecharge.es\/index.php\/2019\/10\/25\/participamos-en-el-xiv-congreso-nacional-del-sindrome-de-cornelia-de-lange\/","title":{"rendered":"Participamos en el XIV Congreso Nacional del S\u00edndrome de Cornelia de Lange"},"content":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: <\/p>\n<p><p>El 25 de octubre comienza en Madrid el XIV Congreso Nacional del S\u00edndrome de Cornelia de Lange, organizado por la Asociaci\u00f3n Espa\u00f1ola del SCdL y por la Direcci\u00f3n General de Pol\u00edticas de Discapacidad. Desde FEDER no nos hemos querido perder la oportunidad de asistir y apoyar al colectivo de pacientes y familiares que conviven con esta condici\u00f3n, es por ello, que nuestro miembro de Junta Directiva, Abraham de las Pe\u00f1as, participar\u00e1 en la inauguraci\u00f3n del evento.<\/p>\n<p>Se trata de un encuentro anual con un doble objetivo: Por un lado, dar a conocer los avances cient\u00edficos y poner sobre la mesa los temas m\u00e9dicos que m\u00e1s preocupan a las familias. Por otro, se establece un punto de encuentro para las familias con un miembro con el SCdL repartidas por el territorio espa\u00f1ol, para que puedan compartir sus experiencias y disminuir el sentimiento de aislamiento, debido a los pocos casos diagnosticados.<\/p>\n<p>A trav\u00e9s de estos congresos se empodera a entidades y familiares ya que, se ofrece conocimientos y experiencias que fortalezcan los lazos de uni\u00f3n entre el colectivo de S\u00edndrome de Cornelia de Lange, ya que solamente, juntos podremos mejorar la calidad de vida de las personas que conviven con alguna enfermedad poco frecuente y construir un futuro donde la esperanza sea la protagonista.<\/p>\n<p><span style=\"font-size: 12pt\">Expertos en investigaci\u00f3n y tratamiento se dan cita en este congreso.<\/span><\/p>\n<p>Un a\u00f1o m\u00e1s, se contar\u00e1 con los referentes en la investigaci\u00f3n y tratamiento del S\u00edndrome Cornelia de Lange. Profesionales del Centro de Referencia del SCdL en Espa\u00f1a, situado en Zaragoza, se desplazar\u00e1n para poner sobre la mesa las \u00faltimas novedades y visitar a las personas afectadas de este s\u00edndrome. De este modo, el Dr. Feliciano J. Ramos, Pediatra Genetista y miembro del comit\u00e9 cient\u00edfico CDSL World, y el Dr. Juan Pie, Genetista Director de la Unidad de Gen\u00e9tica Cl\u00ednica y Gen\u00f3mica Funcional, volver\u00e1n a ser dos de los ponentes m\u00e1s esperados por las familias.<\/p>\n<\/p>\n<p>Fuente: FEDER <a href=\"https:\/\/enfermedades-raras.org\/index.php\/actualidad\/noticias-eventos\/2-feder\/13104-participamos-en-el-xiv-congreso-nacional-del-s%C3%ADndrome-de-cornelia-de-lange\" target=\"_blank\" rel=\"noopener noreferrer\">Participamos en el XIV Congreso Nacional del S\u00edndrome de Cornelia de Lange<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: El 25 de octubre comienza en Madrid el XIV Congreso Nacional del S\u00edndrome de Cornelia de Lange, organizado por la Asociaci\u00f3n Espa\u00f1ola del SCdL y por la Direcci\u00f3n General de Pol\u00edticas de Discapacidad. Desde FEDER no nos hemos querido perder la oportunidad de [&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-4749","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>Participamos en el XIV Congreso Nacional del S\u00edndrome de Cornelia de Lange - 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\/10\/25\/participamos-en-el-xiv-congreso-nacional-del-sindrome-de-cornelia-de-lange\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Participamos en el XIV Congreso Nacional del S\u00edndrome de Cornelia de Lange - 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: El 25 de octubre comienza en Madrid el XIV Congreso Nacional del S\u00edndrome de Cornelia de Lange, organizado por la Asociaci\u00f3n Espa\u00f1ola del SCdL y por la Direcci\u00f3n General de Pol\u00edticas de Discapacidad. 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