{"id":3081,"date":"2020-06-08T19:05:26","date_gmt":"2020-06-08T19:05:26","guid":{"rendered":"http:\/\/alianzapacientes.org\/?p=3081"},"modified":"2020-06-08T19:05:26","modified_gmt":"2020-06-08T19:05:26","slug":"amiloidosis-hereditaria-y-o-enfermedad-de-andrade","status":"publish","type":"post","link":"https:\/\/www.marianakirby.com\/alapa\/2020\/06\/08\/amiloidosis-hereditaria-y-o-enfermedad-de-andrade\/","title":{"rendered":"Amiloidosis Hereditaria y\/o Enfermedad de Andrade"},"content":{"rendered":"<p>\u00bfAmiloidosis Hereditaria (hATTR)? \u00bfEnfermedad de Andrade? \u00bfPolineuropatia Amiloid\u00f3tica Familiar? Diferentes nombres para una enfermedad poco frecuente que este <strong>10 de junio<\/strong> tiene su d\u00eda de conmemoraci\u00f3n en reconocimiento al nacimiento del <strong>Dr. M\u00e1rio Corino Andrade<\/strong>. El portugu\u00e9s describi\u00f3 la Polineuropatia Amiloid\u00f3tica Familiar (PAF) en 1952 y a partir de all\u00ed, comenz\u00f3 a llamarse tambi\u00e9n <strong>Enfermedad de Andrade<\/strong>. Este \u00faltimo nombre junto a <strong>Amiloidosis Hereditaria (hATTR)<\/strong> son los recomendados para usar actualmente.<br \/>\nSe trata de una enfermedad poco frecuente, hereditaria, progresiva y de dif\u00edcil diagn\u00f3stico que produce una degeneraci\u00f3n del sistema nervioso.<\/p>\n<p>&nbsp;<\/p>\n<figure id=\"attachment_3082\" aria-describedby=\"caption-attachment-3082\" style=\"width: 349px\" class=\"wp-caption aligncenter\"><img fetchpriority=\"high\" decoding=\"async\" class=\"wp-image-3082\" src=\"http:\/\/alianzapacientes.org\/wp-content\/uploads\/2020\/06\/AMILOIDOSIS-300x300.jpg\" alt=\"D\u00eda Mundial de la Enfermedad de Andrade - Amiloidosis Hereditaria\" width=\"349\" height=\"349\" \/><figcaption id=\"caption-attachment-3082\" class=\"wp-caption-text\">D\u00eda Mundial de la Enfermedad de Andrade &#8211; Amiloidosis Hereditaria<\/figcaption><\/figure>\n<p>&nbsp;<\/p>\n<p>En nuestro pa\u00eds, el <a href=\"https:\/\/www.facebook.com\/amiloidosisargentina\/\" target=\"_blank\" rel=\"noopener noreferrer\">Grupo Argentino de Amiloidosis<\/a> junto a la <strong>Alianza Argentina de Pacientes \u2013 ALAPA<\/strong>, han planificado algunas actividades para pacientes y profesionales de la salud.<br \/>\nEste <strong>mi\u00e9rcoles 10 de junio a las 17 horas<\/strong>, la Licenciada en Nutrici\u00f3n, <strong>Marilina Beron<\/strong> (Matr\u00edcula Nacional 6766) brindar\u00e1 una charla para <strong>pacientes<\/strong>\u00a0y sus <strong>familiares<\/strong> a trav\u00e9s de la plataforma <strong>Zoom<\/strong>. El ID para acceder es <strong>785 613 1222<\/strong>.<\/p>\n<p>&nbsp;<\/p>\n<figure id=\"attachment_3015\" aria-describedby=\"caption-attachment-3015\" style=\"width: 349px\" class=\"wp-caption aligncenter\"><img decoding=\"async\" class=\"wp-image-3015\" src=\"http:\/\/alianzapacientes.org\/wp-content\/uploads\/2020\/06\/1ENCUENTRO-AMILOIDOSIS-300x300.jpg\" alt=\"Flyer del evento Encuentro de Pacientes con Amiloidosis Hereditaria\" width=\"349\" height=\"349\" \/><figcaption id=\"caption-attachment-3015\" class=\"wp-caption-text\">Encuentro de Pacientes con Amiloidosis Hereditaria<\/figcaption><\/figure>\n<p>&nbsp;<\/p>\n<p><strong>Andrea Frione<\/strong>, coordinadora del <strong>Grupo Argentino de Amiloidosis<\/strong>, indic\u00f3: <em>\u201ces muy importante conmemorar nuestro d\u00eda porque de esta forma hacemos visible a esta enfermedad que muy pocas personas conocen en el mundo. As\u00ed podemos llegar a que m\u00e1s gente la reconozca y encontrar a m\u00e1s personas sin diagn\u00f3stico ni tratamiento\u201d<\/em>.<\/p>\n<p>&nbsp;<\/p>\n<p><iframe title=\"Andrea Frione - Amiloidosis\" width=\"800\" height=\"450\" src=\"https:\/\/www.youtube.com\/embed\/YId6C6Gxvok?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture; web-share\" referrerpolicy=\"strict-origin-when-cross-origin\" allowfullscreen><\/iframe><\/p>\n<p>&nbsp;<\/p>\n<p>Adem\u00e1s, y con el objetivo de brindar herramientas a la <strong>comunidad m\u00e9dica latinoamericana<\/strong>, el <strong>3 de julio a las 15.00 horas<\/strong> (de la <strong>Argentina<\/strong>) se llevar\u00e1 a cabo la <strong>Jornada \u201cEntendiendo hATTR\u201d &#8211; Amiloidosis ATTR Hereditaria \u2013 Enfermedad de Andrade<\/strong> a trav\u00e9s de la plataforma <strong>Zoom<\/strong>. ID: <strong>785 613 1222<\/strong>.<br \/>\nDisertar\u00e1n la <strong>Dra. Valeria Saluto<\/strong> (neur\u00f3loga &#8211; MN 122544), la <strong>Dra. Gisela Streitenberger<\/strong> (cardi\u00f3loga &#8211; MN 116239) y el <strong>Dr. Agust\u00edn Manchado<\/strong> (medico cl\u00ednico &#8211; MN 152398).<\/p>\n<p>&nbsp;<\/p>\n<h3><span style=\"color: #800080;\"><strong>S\u00edntomas<\/strong><\/span><\/h3>\n<p>Desde el <a href=\"https:\/\/www.facebook.com\/amiloidosisargentina\/\" target=\"_blank\" rel=\"noopener noreferrer\">Grupo Argentino de Amiloidosis<\/a> afirmaron que en la actualidad cuentan con 150 pacientes detectados en el territorio nacional.<br \/>\nPara poder llegar a m\u00e1s personas, es fundamental conocer cu\u00e1les son los signos y s\u00edntomas m\u00e1s comunes.<br \/>\nLo primero que hay que saber es que la aparici\u00f3n, normalmente, se da entre los 30 y 50 a\u00f1os, tanto en hombres como en mujeres, y que en cada caso los s\u00edntomas pueden variar.<\/p>\n<p>&nbsp;<\/p>\n<p><iframe title=\"Rocio - Amiloidosis Hereditaria\" width=\"800\" height=\"450\" src=\"https:\/\/www.youtube.com\/embed\/AmW7AYR3fE8?feature=oembed\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture; web-share\" referrerpolicy=\"strict-origin-when-cross-origin\" allowfullscreen><\/iframe><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<ul>\n<li>Gastrointestinalmente se dan diarreas, p\u00e9rdida de peso sin motivo evidente, n\u00e1useas y estre\u00f1imiento.<\/li>\n<li>Los s\u00edntomas genitourinarios son impotencia sexual, incontinencia urinaria y retenci\u00f3n urinaria.<\/li>\n<li>Los s\u00edntomas del sistema nervioso son punzadas, sensaci\u00f3n de quemaz\u00f3n u hormigueo, que inicia en los pies y va ascendiendo por las piernas, p\u00e9rdida de fuerza de los miembros inferiores y de sensibilidad al dolor y a la temperatura. Adem\u00e1s, ausencia de dolor ante quemaduras, heridas o golpes, principalmente en miembros inferiores.<\/li>\n<li>Los s\u00edntomas cardiovasculares m\u00e1s frecuentes son desmayos, mareos, fatiga, palpitaciones y pies o piernas hinchadas.<\/li>\n<li>En la visi\u00f3n, los s\u00edntomas son \u00falceras en la c\u00f3rnea, ojo seco, disminuci\u00f3n de la visi\u00f3n nocturna y visi\u00f3n borrosa.<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>\u00bfAmiloidosis Hereditaria (hATTR)? \u00bfEnfermedad de Andrade? \u00bfPolineuropatia Amiloid\u00f3tica Familiar? Diferentes nombres para una enfermedad poco frecuente que este 10 de junio tiene su d\u00eda de conmemoraci\u00f3n en reconocimiento al nacimiento del Dr. M\u00e1rio Corino Andrade. El portugu\u00e9s describi\u00f3 la Polineuropatia Amiloid\u00f3tica Familiar (PAF) en 1952 y a partir de all\u00ed, comenz\u00f3 a llamarse tambi\u00e9n Enfermedad [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":3085,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_joinchat":[],"footnotes":""},"categories":[7],"tags":[],"class_list":["post-3081","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-enfermedades-poco-frecuentes"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Amiloidosis Hereditaria y\/o Enfermedad de Andrade - 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\/08\/amiloidosis-hereditaria-y-o-enfermedad-de-andrade\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Amiloidosis Hereditaria y\/o Enfermedad de Andrade - Alianza Argentina de Pacientes - ALAPA\" \/>\n<meta property=\"og:description\" content=\"\u00bfAmiloidosis Hereditaria (hATTR)? \u00bfEnfermedad de Andrade? \u00bfPolineuropatia Amiloid\u00f3tica Familiar? Diferentes nombres para una enfermedad poco frecuente que este 10 de junio tiene su d\u00eda de conmemoraci\u00f3n en reconocimiento al nacimiento del Dr. M\u00e1rio Corino Andrade. El portugu\u00e9s describi\u00f3 la Polineuropatia Amiloid\u00f3tica Familiar (PAF) en 1952 y a partir de all\u00ed, comenz\u00f3 a llamarse tambi\u00e9n Enfermedad [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marianakirby.com\/alapa\/2020\/06\/08\/amiloidosis-hereditaria-y-o-enfermedad-de-andrade\/\" \/>\n<meta property=\"og:site_name\" content=\"Alianza Argentina de Pacientes - ALAPA\" \/>\n<meta property=\"article:published_time\" content=\"2020-06-08T19:05:26+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.marianakirby.com\/alapa\/wp-content\/uploads\/2020\/06\/Portada-nota-amiloidosis.fw_.png\" \/>\n\t<meta property=\"og:image:width\" content=\"960\" \/>\n\t<meta property=\"og:image:height\" content=\"542\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Mary\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Escrito por\" \/>\n\t<meta name=\"twitter:data1\" content=\"Mary\" \/>\n\t<meta name=\"twitter:label2\" content=\"Tiempo de lectura\" \/>\n\t<meta name=\"twitter:data2\" content=\"3 minutos\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marianakirby.com\\\/alapa\\\/2020\\\/06\\\/08\\\/amiloidosis-hereditaria-y-o-enfermedad-de-andrade\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marianakirby.com\\\/alapa\\\/2020\\\/06\\\/08\\\/amiloidosis-hereditaria-y-o-enfermedad-de-andrade\\\/\"},\"author\":{\"name\":\"Mary\",\"@id\":\"https:\\\/\\\/www.marianakirby.com\\\/alapa\\\/#\\\/schema\\\/person\\\/760e027a6f84dbb2308cc52837bafcee\"},\"headline\":\"Amiloidosis Hereditaria y\\\/o Enfermedad de Andrade\",\"datePublished\":\"2020-06-08T19:05:26+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marianakirby.com\\\/alapa\\\/2020\\\/06\\\/08\\\/amiloidosis-hereditaria-y-o-enfermedad-de-andrade\\\/\"},\"wordCount\":567,\"image\":{\"@id\":\"https:\\\/\\\/www.marianakirby.com\\\/alapa\\\/2020\\\/06\\\/08\\\/amiloidosis-hereditaria-y-o-enfermedad-de-andrade\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.marianakirby.com\\\/alapa\\\/wp-content\\\/uploads\\\/2020\\\/06\\\/Portada-nota-amiloidosis.fw_.png\",\"articleSection\":[\"Enfermedades Poco Frecuentes\"],\"inLanguage\":\"es-AR\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marianakirby.com\\\/alapa\\\/2020\\\/06\\\/08\\\/amiloidosis-hereditaria-y-o-enfermedad-de-andrade\\\/\",\"url\":\"https:\\\/\\\/www.marianakirby.com\\\/alapa\\\/2020\\\/06\\\/08\\\/amiloidosis-hereditaria-y-o-enfermedad-de-andrade\\\/\",\"name\":\"Amiloidosis Hereditaria y\\\/o Enfermedad de Andrade - 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