{"id":2114,"date":"2018-09-21T10:20:23","date_gmt":"2018-09-21T10:20:23","guid":{"rendered":"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2018\/09\/21\/presentacion\/"},"modified":"2026-03-02T12:02:27","modified_gmt":"2026-03-02T12:02:27","slug":"presentacion","status":"publish","type":"post","link":"https:\/\/exciting-elbakyan.137-74-93-36.plesk.page\/index.php\/2018\/09\/21\/presentacion\/","title":{"rendered":"Presentaci\u00f3n"},"content":{"rendered":"<p style=\"text-align: justify;\"><strong><span style=\"font-size: 14pt;\">La ataxia telangiectasia es una enfermedad rara, gen\u00e9tica y neurodegenerativa que a\u00fan no tiene cura ni tratamiento.<\/span><\/strong><\/p>\n<p style=\"text-align: justify;\"><strong><span style=\"font-size: 14pt;\">Causa una grave discapacidad f\u00edsica progresiva, inmunodeficiencia, problemas respiratorios frecuentes y una mayor predisposici\u00f3n al c\u00e1ncer.&nbsp;<\/span><\/strong><\/p>\n<p style=\"text-align: justify;\"><strong><span style=\"font-size: 14pt;\"><span style=\"color: #ff00ff;\">AEFAT<\/span>, asociaci\u00f3n creada en 2009, agrupa a unas 40 familias con afectados en Espa\u00f1a, en su mayor\u00eda ni\u00f1os y j\u00f3venes.<\/span><\/strong><\/p>\n<p style=\"text-align: justify;\"><strong><span style=\"font-size: 14pt;\">Luchamos por la investigaci\u00f3n de esta enfermedad rara, financiando proyectos de investigaci\u00f3n.<\/span><\/strong><\/p>\n<p style=\"text-align: justify;\"><strong><span style=\"font-size: 14pt;\">Buscamos una mejor calidad de vida para nuestros hijos y queremos sensibilizar a la sociedad para lograr una mayor inclusi\u00f3n.<\/span><\/strong><\/p>\n<p style=\"text-align: justify;\"><strong><span style=\"font-size: 14pt;\">\u00bfNos ayudas?<\/span><\/strong><\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>La ataxia telangiectasia es una enfermedad rara, gen\u00e9tica y neurodegenerativa que a\u00fan no tiene cura ni tratamiento. Causa una grave discapacidad f\u00edsica progresiva, inmunodeficiencia, problemas respiratorios frecuentes y una mayor predisposici\u00f3n al c\u00e1ncer.&nbsp; AEFAT, asociaci\u00f3n creada en 2009, agrupa a unas 40 familias con afectados en Espa\u00f1a, en su mayor\u00eda ni\u00f1os y j\u00f3venes. Luchamos por [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":true,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[809],"tags":[],"class_list":["post-2114","post","type-post","status-publish","format-standard","hentry","category-sin-categoria"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Presentaci\u00f3n - 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=\"Presentaci\u00f3n - Aefat\" \/>\n<meta property=\"og:description\" content=\"La ataxia telangiectasia es una enfermedad rara, gen\u00e9tica y neurodegenerativa que a\u00fan no tiene cura ni tratamiento. 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