{"id":2034,"date":"2016-11-11T12:38:18","date_gmt":"2016-11-11T12:38:18","guid":{"rendered":"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2016\/11\/11\/vi-encuentro-anual-de-aefat-en-el-creer-de-burgos\/"},"modified":"2026-03-02T12:02:38","modified_gmt":"2026-03-02T12:02:38","slug":"vi-encuentro-anual-de-aefat-en-el-creer-de-burgos","status":"publish","type":"post","link":"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2016\/11\/11\/vi-encuentro-anual-de-aefat-en-el-creer-de-burgos\/","title":{"rendered":"VI encuentro anual de AEFAT en el CREER de Burgos"},"content":{"rendered":"<p><span style=\"font-size: 12pt;\">El pasado fin de semana se celebr\u00f3 en el CREER de Burgos el VI encuentro de AEFAT, la asociaci\u00f3n que agrupa a las familias afectadas por ataxia-telangiectasia.<\/span><\/p>\n<p><span style=\"font-size: 12pt;\"><img decoding=\"async\" class=\" alignleft size-full wp-image-2033\" src=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2016\/11\/38_centro_enfermedades_raras.jpg\" alt=\"38 centro enfermedades raras\" style=\"margin-right: 10px; margin-bottom: 10px; float: left;\" width=\"200\" height=\"150\" srcset=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2016\/11\/38_centro_enfermedades_raras.jpg 200w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2016\/11\/38_centro_enfermedades_raras-16x12.jpg 16w\" sizes=\"(max-width: 200px) 100vw, 200px\" \/><\/span><\/p>\n<p><span style=\"font-size: 12pt;\">La AT es una enfermedad de las consideradas raras o poco frecuentes y que afecta a unos 30 ni\u00f1os y ni\u00f1as en todo el estado, entre ellos dos hermanos burgaleses: Adri\u00e1n y B\u00e1rbara. La enfermedad, que es altamente incapacitante, cursa con un deterioro progresivo de la capacidad motora adem\u00e1s de otras complicaciones como inmunodeficiencia y una mayor probabilidad de desarrollo de linfomas y leucemias.<\/span><br \/><span style=\"font-size: 12pt;\">Durante el encuentro, adem\u00e1s de actividades l\u00fadicas como la visita al Museo de la Evoluci\u00f3n Humana, se han desarrollado dos ponencias, una primera para explicar a las familias las conclusiones del \u00faltimo congreso que sobre AT se ha celebrado en<\/span><br \/><span style=\"font-size: 12pt;\">Polonia. Para la segunda ponencia las familias han contado con la presencia de Almudena Serrano, investigadora del CABIMER y receptora de la 1\u00aa beca predoctoral AEFAT. <\/span><\/p>\n<p><span style=\"font-size: 12pt;\">Esta beca pretende impulsar la investigaci\u00f3n de la AT y ha sido posible gracias a la recaudaci\u00f3n obtenida en las diferentes actividades de la asociaci\u00f3n, entre ellas la 1\u00aa Gala Solidaria \u201c\u00a1T\u00fa s\u00ed que eres raro!\u201d, organizada el a\u00f1o pasado por la asociaci\u00f3n burgalesa \u201cQue la Sierra Baile\u201d(entidad organizadora del festival DEMANDAFOLK). Este evento const\u00f3 de un pasabares por el centro de la ciudad y un festival de Folk y Circo (con las actuaciones de los Terapiclowns, Parradust y Diego Galaz y amigos) en la casa de la cultura de Gamonal y consigui\u00f3 recaudar m\u00e1s de 3000\u20ac. En palabras de Almudena Serrano&#8230;\u201dgracias a AEFAT estamos estudiando la posible contribuci\u00f3n de las roturas bloqueadas de ADN en la patog\u00e9nesis de la ataxia-telangiectasia. \u201d<\/span><br \/><span style=\"font-size: 12pt;\">La asociaci\u00f3n se encuentra inmersa en dos nuevos proyectos: por un lado la resoluci\u00f3n de una nueva convocatoria de beca predoctoral y por otro la participaci\u00f3n en un ambicioso proyecto que pretende crear una base de datos de pacientes a nivel mundial con el fin de obtener informaci\u00f3n suficiente para cruzar datos que permitan obtener un mejor conocimiento de la enfermedad. Y es que seg\u00fan apunta Nadia, madre de uno de los peque\u00f1os afectados, todos los esfuerzos son pocos para intentar avanzar en la investigaci\u00f3n de la enfermedad que afecta a nuestros hijos.<\/span><\/p>\n<p><span style=\"font-size: 12pt;\"><a href=\"http:\/\/www.noticiasburgos.com\/Hemeroteca2\/tabid\/303\/ctl\/ArticleView\/mid\/777\/articleId\/23982\/I-encuentro-anual-de-AEFAT-en-el-CREER-de-Burgos.aspx\">http:\/\/www.noticiasburgos.com\/Hemeroteca2\/tabid\/303\/ctl\/ArticleView\/mid\/777\/articleId\/23982\/I-encuentro-anual-de-AEFAT-en-el-CREER-de-Burgos.aspx<\/a><\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p><span style=\"font-size: 12pt;\">El pasado fin de semana se celebr\u00f3 en el CREER de Burgos el VI encuentro de AEFAT, la asociaci\u00f3n que agrupa a las familias afectadas por ataxia-telangiectasia.<\/span><\/p>\n<p><span style=\"font-size: 12pt;\"><img decoding=\"async\" class=\" alignleft size-full wp-image-2033\" src=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2016\/11\/38_centro_enfermedades_raras.jpg\" alt=\"38 centro enfermedades raras\" style=\"margin-right: 10px; margin-bottom: 10px; float: left;\" width=\"200\" height=\"150\" srcset=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2016\/11\/38_centro_enfermedades_raras.jpg 200w, https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2016\/11\/38_centro_enfermedades_raras-16x12.jpg 16w\" sizes=\"(max-width: 200px) 100vw, 200px\" \/><\/span><\/p>\n<p><span style=\"font-size: 12pt;\">La AT es una enfermedad de las consideradas raras o poco frecuentes y que afecta a unos 30 ni\u00f1os y ni\u00f1as en todo el estado, entre ellos dos hermanos burgaleses: Adri\u00e1n y B\u00e1rbara. La enfermedad, que es altamente incapacitante, cursa con un deterioro progresivo de la capacidad motora adem\u00e1s de otras complicaciones como inmunodeficiencia y una mayor probabilidad de desarrollo de linfomas y leucemias.<\/span><br \/><span style=\"font-size: 12pt;\">Durante el encuentro, adem\u00e1s de actividades l\u00fadicas como la visita al Museo de la Evoluci\u00f3n Humana, se han desarrollado dos ponencias, una primera para explicar a las familias las conclusiones del \u00faltimo congreso que sobre AT se ha celebrado en<\/span><br \/><span style=\"font-size: 12pt;\">Polonia. Para la segunda ponencia las familias han contado con la presencia de Almudena Serrano, investigadora del CABIMER y receptora de la 1\u00aa beca predoctoral AEFAT. <\/span><\/p>\n","protected":false},"author":1,"featured_media":2033,"comment_status":"closed","ping_status":"open","sticky":true,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[809],"tags":[107,108,170],"class_list":["post-2034","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-sin-categoria","tag-creer","tag-encuentro","tag-encuentro-aefat"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>VI encuentro anual de AEFAT en el CREER de Burgos - Aefat<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"VI encuentro anual de AEFAT en el CREER de Burgos - Aefat\" \/>\n<meta property=\"og:description\" content=\"El pasado fin de semana se celebr\u00f3 en el CREER de Burgos el VI encuentro de AEFAT, la asociaci\u00f3n que agrupa a las familias afectadas por ataxia-telangiectasia.  La AT es una enfermedad de las consideradas raras o poco frecuentes y que afecta a unos 30 ni\u00f1os y ni\u00f1as en todo el estado, entre ellos dos hermanos burgaleses: Adri\u00e1n y B\u00e1rbara. La enfermedad, que es altamente incapacitante, cursa con un deterioro progresivo de la capacidad motora adem\u00e1s de otras complicaciones como inmunodeficiencia y una mayor probabilidad de desarrollo de linfomas y leucemias.Durante el encuentro, adem\u00e1s de actividades l\u00fadicas como la visita al Museo de la Evoluci\u00f3n Humana, se han desarrollado dos ponencias, una primera para explicar a las familias las conclusiones del \u00faltimo congreso que sobre AT se ha celebrado enPolonia. Para la segunda ponencia las familias han contado con la presencia de Almudena Serrano, investigadora del CABIMER y receptora de la 1\u00aa beca predoctoral AEFAT.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2016\/11\/11\/vi-encuentro-anual-de-aefat-en-el-creer-de-burgos\/\" \/>\n<meta property=\"og:site_name\" content=\"Aefat\" \/>\n<meta property=\"article:published_time\" content=\"2016-11-11T12:38:18+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2026-03-02T12:02:38+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2016\/11\/38_centro_enfermedades_raras.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"200\" \/>\n\t<meta property=\"og:image:height\" content=\"150\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"admin\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Escrito por\" \/>\n\t<meta name=\"twitter:data1\" content=\"admin\" \/>\n\t<meta name=\"twitter:label2\" content=\"Tiempo de lectura\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutos\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2016\/11\/11\/vi-encuentro-anual-de-aefat-en-el-creer-de-burgos\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2016\/11\/11\/vi-encuentro-anual-de-aefat-en-el-creer-de-burgos\/\"},\"author\":{\"name\":\"admin\",\"@id\":\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/#\/schema\/person\/d75277649f873b670821832f92709a5f\"},\"headline\":\"VI encuentro anual de AEFAT en el CREER de Burgos\",\"datePublished\":\"2016-11-11T12:38:18+00:00\",\"dateModified\":\"2026-03-02T12:02:38+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2016\/11\/11\/vi-encuentro-anual-de-aefat-en-el-creer-de-burgos\/\"},\"wordCount\":415,\"publisher\":{\"@id\":\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/#organization\"},\"image\":{\"@id\":\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2016\/11\/11\/vi-encuentro-anual-de-aefat-en-el-creer-de-burgos\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/wp-content\/uploads\/2016\/11\/38_centro_enfermedades_raras.jpg\",\"keywords\":[\"CREER\",\"encuentro\",\"Encuentro AEFAT\"],\"inLanguage\":\"es\"},{\"@type\":\"WebPage\",\"@id\":\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2016\/11\/11\/vi-encuentro-anual-de-aefat-en-el-creer-de-burgos\/\",\"url\":\"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2016\/11\/11\/vi-encuentro-anual-de-aefat-en-el-creer-de-burgos\/\",\"name\":\"VI encuentro anual de AEFAT en el CREER de Burgos - 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