{"id":6296,"date":"2020-10-22T07:11:34","date_gmt":"2020-10-22T07:11:34","guid":{"rendered":"https:\/\/sindromecharge.es\/index.php\/2020\/10\/22\/la-asociacion-espanola-del-sindrome-cornelia-de-lange-organiza-su-xv-congreso-nacional-cientifico-familiar\/"},"modified":"2020-10-22T07:11:34","modified_gmt":"2020-10-22T07:11:34","slug":"la-asociacion-espanola-del-sindrome-cornelia-de-lange-organiza-su-xv-congreso-nacional-cientifico-familiar","status":"publish","type":"post","link":"https:\/\/sindromecharge.es\/index.php\/2020\/10\/22\/la-asociacion-espanola-del-sindrome-cornelia-de-lange-organiza-su-xv-congreso-nacional-cientifico-familiar\/","title":{"rendered":"La Asociaci\u00f3n Espa\u00f1ola del S\u00edndrome Cornelia de Lange organiza su XV Congreso Nacional Cient\u00edfico-Familiar"},"content":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: <\/p>\n<p><p>La Asociaci\u00f3n S\u00edndrome de Cornelia de Lange Espa\u00f1a organiza el 23 y 24 de octubre su XV Congreso Nacional Cient\u00edfico-Familiar Virtual en el que se dar\u00e1n cita expertos en el abordaje de esta enfermedad poco frecuente y familias para impulsar el empoderamiento y el conocimiento sobre esta patolog\u00eda.<\/p>\n<p>En esta ocasi\u00f3n, Abraham de las Pe\u00f1as, Vocal de la Junta Directiva de nuestra Federaci\u00f3n inaugurar\u00e1 junto a Ana Ma. Garcia Presidenta de la entidad. Adem\u00e1s, se hablar\u00e1 sobre testamento y patrimonio protegido, la actualizaci\u00f3n cl\u00ednica de la patolog\u00eda, las nuevas relaciones genotipo-fenotipo, la aplicacion del reconocimiento facial en el diagn\u00f3stico cl\u00ednico, las caracteristicas de las distintas muestras biol\u00f3gicas, el diagn\u00f3stico gen\u00e9tico, la importancia del mosaicismo, la nueva mutaci\u00f3n en el gen SETD5, el comportamiento y el bienestar de ni\u00f1os y adunltos y los problemas comunes del tracto gastrointestinal.<\/p>\n<p>Desde FEDER aplaudimos encuentros como este, ya que a trav\u00e9s de la puesta en com\u00fan de experiencias y conocimiento se puede avanzar hacia un futuro donde la ilusi\u00f3n y la esperanza son las protagonistas.<\/p>\n<p>Si quieres conocer m\u00e1s sobre este encuentro, te adjuntamos en la parte superior de la noticia, el programa del XV Congreso Nacional.<\/p>\n<p>\u00daltima actualizaci\u00f3n 21\/10\/2020<\/p>\n<p>&nbsp;<\/p>\n<\/p>\n<p>Fuente: FEDER <a href=\"https:\/\/enfermedades-raras.org\/index.php\/actualidad\/noticias-eventos\/2-feder\/14414-la-asociaci%C3%B3n-espa%C3%B1ola-del-s%C3%ADndrome-cornelia-de-lange-organiza-su-xv-congreso-nacional-cient%C3%ADfico-familiar\" target=\"_blank\" rel=\"noopener noreferrer\">La Asociaci\u00f3n Espa\u00f1ola del S\u00edndrome Cornelia de Lange organiza su XV Congreso Nacional Cient\u00edfico-Familiar<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Leemos en FEDER la siguiente noticia que os reproducimos de forma \u00edntegra: La Asociaci\u00f3n S\u00edndrome de Cornelia de Lange Espa\u00f1a organiza el 23 y 24 de octubre su XV Congreso Nacional Cient\u00edfico-Familiar Virtual en el que se dar\u00e1n cita expertos en el abordaje de esta enfermedad poco frecuente y familias para impulsar el empoderamiento y [&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-6296","post","type-post","status-publish","format-standard","hentry","category-noticias","tag-enfermedades-raras"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - 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