{"id":3096,"date":"2020-06-19T18:08:58","date_gmt":"2020-06-19T18:08:58","guid":{"rendered":"http:\/\/alianzapacientes.org\/?p=3096"},"modified":"2020-06-19T18:08:58","modified_gmt":"2020-06-19T18:08:58","slug":"entendiendo-hattr","status":"publish","type":"post","link":"https:\/\/www.marianakirby.com\/alapa\/2020\/06\/19\/entendiendo-hattr\/","title":{"rendered":"Jornada sobre Amiloidosis Hereditaria"},"content":{"rendered":"<p>La <strong>Alianza Argentina de Pacientes \u2013 ALAPA<\/strong> y el <a href=\"https:\/\/www.facebook.com\/amiloidosisargentina\/\" target=\"_blank\" rel=\"noopener noreferrer\"><strong>Grupo Argentino de Amiloidosis<\/strong><\/a> convocan a la comunidad m\u00e9dica latinoamericana a participar en la jornada <strong>\u201cEntendiendo hATTR: Amiloidosis Hereditaria \u2013 Enfermedad de Andrade\u201d<\/strong> que se desarrollar\u00e1 el <strong>viernes 3 de julio<\/strong> a las <strong>18.00 horas (Argentina)<\/strong> a trav\u00e9s de la plataforma <strong>Zoom<\/strong>. El ID para acceder a la misma es <strong>7856131222<\/strong>.<\/p>\n<p>La charla estar\u00e1 a cargo de la <strong>Dra. Valeria Saluto<\/strong>, (neur\u00f3loga \u2013 Matr\u00edcula Nacional 122.544), la <strong>Dra. Gisela Streitenberger<\/strong> (cardi\u00f3loga &#8211; Matr\u00edcula Nacional 116.239) y el <strong>Dr. Agust\u00edn Manchado<\/strong> (m\u00e9dico cl\u00ednico &#8211; Matr\u00edcula Nacional 152.398).<\/p>\n<p>&nbsp;<\/p>\n<figure id=\"attachment_3136\" aria-describedby=\"caption-attachment-3136\" style=\"width: 349px\" class=\"wp-caption aligncenter\"><img fetchpriority=\"high\" decoding=\"async\" class=\"wp-image-3136\" src=\"http:\/\/alianzapacientes.org\/wp-content\/uploads\/2020\/06\/ENTENDIENDO-HATTR-1-300x300.jpg\" alt=\"Entendiendo hATTR - Amoloidosis Hereditaria\" width=\"349\" height=\"347\" \/><figcaption id=\"caption-attachment-3136\" class=\"wp-caption-text\">Entendiendo hATTR &#8211; Amoloidosis Hereditaria<\/figcaption><\/figure>\n<p>&nbsp;<\/p>\n<p>La <strong>Dra. Saluto<\/strong> es neur\u00f3loga del Instituto de Investigaciones M\u00e9dicas Alfredo Lanari &#8211; Universidad de Buenos Aires. La <strong>Dra. Streitenberger<\/strong> es m\u00e9dica cardi\u00f3loga de planta de Unidad Coronaria, Consultorios externos de Cardiolog\u00eda y Ecocardiograf\u00eda del Hospital \u201cEl Cruce\u201d de Florencio Varela. Por su lado, el <strong>Dr. Manchado<\/strong> es m\u00e9dico cl\u00ednico del Instituto de Investigaciones M\u00e9dicas Alfredo Lanari &#8211; Universidad de Buenos Aires.<\/p>\n<p>&nbsp;<\/p>\n<h3><span style=\"color: #800080;\"><strong>Objetivos de la jornada<\/strong><\/span><\/h3>\n<p><strong><img decoding=\"async\" class=\" wp-image-3098 alignleft\" src=\"http:\/\/alianzapacientes.org\/wp-content\/uploads\/2020\/06\/va-300x251.png\" alt=\"\" width=\"260\" height=\"217\" srcset=\"https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/06\/va-300x251.png 300w, https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/06\/va-1024x857.png 1024w, https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/06\/va-768x643.png 768w, https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/06\/va.png 1043w\" sizes=\"(max-width: 260px) 100vw, 260px\" \/>Carolina Oliveto<\/strong>, <strong>directora Gral. de Programas de ALAPA<\/strong>, cont\u00f3 c\u00f3mo surgi\u00f3 esta iniciativa. \u201cCreemos de suma importancia organizar un webinario a nivel latinoamericano para concientizar sobre Amiloidosis Hereditaria ya que es una de las 8 mil enfermedades poco frecuentes. Queremos que la comunidad m\u00e9dica sospeche esta enfermedad. Una persona con un diagn\u00f3stico temprano, puede llegar a un tratamiento adecuado y, sobretodo, se evita que avance la enfermedad. Hoy en d\u00eda no hay cura pero s\u00ed hay tratamientos. Necesitamos encontrar a los pacientes con esta enfermedad a tiempo. El diagn\u00f3stico precoz es super importante y si llegamos tarde, las chances de evitar el avance son pocas\u201d, detall\u00f3.<\/p>\n<p>Sobre la Amiloidosis Hereditaria explic\u00f3: \u201cse trata de una enfermedad gen\u00e9tica y hereditaria, su transmisi\u00f3n es dominante, es decir que si una persona padece la patolog\u00eda, cada vez que tiene un hijo hay un 50% de posibilidades de transmitir la mutaci\u00f3n a ese hijo\u201d.<\/p>\n<p>Por \u00faltimo, respecto a la situaci\u00f3n regional actual agreg\u00f3: \u201cen la Argentina, por suerte, tenemos acceso a los tratamientos, pero no en toda Am\u00e9rica Latina es as\u00ed. Hay pa\u00edses en los que ni siquiera est\u00e1 aprobado un tratamiento para esta patolog\u00eda. Y como decimos siempre, no se sospecha lo que no se conoce, por eso son importantes estas actividades. Creemos que hay much\u00edsimos pacientes que a\u00fan no llegaron al diagn\u00f3stico y a nivel latinoamericano, se sabe muy poco de esta enfermedad\u201d.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>La Alianza Argentina de Pacientes \u2013 ALAPA y el Grupo Argentino de Amiloidosis convocan a la comunidad m\u00e9dica latinoamericana a participar en la jornada \u201cEntendiendo hATTR: Amiloidosis Hereditaria \u2013 Enfermedad de Andrade\u201d que se desarrollar\u00e1 el viernes 3 de julio a las 18.00 horas (Argentina) a trav\u00e9s de la plataforma Zoom. El ID para acceder [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":3099,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_joinchat":[],"footnotes":""},"categories":[7,8],"tags":[],"class_list":["post-3096","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-enfermedades-poco-frecuentes","category-salud"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Jornada sobre Amiloidosis Hereditaria - Alianza Argentina de Pacientes - ALAPA<\/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:\/\/www.marianakirby.com\/alapa\/2020\/06\/19\/entendiendo-hattr\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Jornada sobre Amiloidosis Hereditaria - Alianza Argentina de Pacientes - ALAPA\" \/>\n<meta property=\"og:description\" content=\"La Alianza Argentina de Pacientes \u2013 ALAPA y el Grupo Argentino de Amiloidosis convocan a la comunidad m\u00e9dica latinoamericana a participar en la jornada \u201cEntendiendo hATTR: Amiloidosis Hereditaria \u2013 Enfermedad de Andrade\u201d que se desarrollar\u00e1 el viernes 3 de julio a las 18.00 horas (Argentina) a trav\u00e9s de la plataforma Zoom. 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