{"id":301,"date":"2014-03-26T22:42:23","date_gmt":"2014-03-26T21:42:23","guid":{"rendered":"http:\/\/s519078666.onlinehome.fr\/?page_id=301"},"modified":"2015-04-08T14:52:59","modified_gmt":"2015-04-08T13:52:59","slug":"understanding-the-disease","status":"publish","type":"page","link":"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/","title":{"rendered":"Understanding the disease"},"content":{"rendered":"<h2>Stargardt disease : an orphan disease<\/h2>\n<p><strong>\u00a0<\/strong><\/p>\n<p><strong>Stargardt disease is a hereditary orphan disease which affects the macula, the central retina area.<\/strong><\/p>\n<p>Reported for the first time by Karl Bruno Stargardt in 1909, Stargardt disease is a progressive deterioration of the macula, named macular dystrophy or maculopathy which, in most cases, appears before the age of 20. It then results in a degenerative loss of acuity and central vision in both eyes. Detail perception and recognition of red-green colours are impaired.<\/p>\n<p>The peripheral retina remains functional all life-long (except in rare cases); the field of vision is preserved which enables patients to remain independent.<\/p>\n<p>No treatments exist for now.<\/p>\n<h3><strong>Hope<\/strong>: Research is developing and clinical trials are underway.<\/h3>\n<div style=\"padding-bottom:20px; padding-top:10px;valign:middle;\" class=\"hupso-share-buttons\"><!-- Hupso Share Buttons - https:\/\/www.hupso.com\/share\/ --><a class=\"hupso_toolbar\" href=\"https:\/\/www.hupso.com\/share\/\"><img src=\"https:\/\/static.hupso.com\/share\/buttons\/share-medium.png\" rel=\"PrettyPhoto[301]\" style=\"border:0px; padding-top: 5px; float:left;\" alt=\"Share Button\"\/><\/a><script type=\"text\/javascript\">var hupso_services_t=new Array(\"Twitter\",\"Facebook\",\"Google Plus\",\"Linkedin\",\"Email\");var hupso_background_t=\"#EAF4FF\";var hupso_border_t=\"#66CCFF\";var hupso_toolbar_size_t=\"medium\";var hupso_image_folder_url = \"\";var hupso_url_t=\"\";var hupso_title_t=\"Understanding%20the%20disease\";<\/script><script type=\"text\/javascript\" src=\"https:\/\/static.hupso.com\/share\/js\/share_toolbar.js\"><\/script><!-- Hupso Share Buttons --><\/div>","protected":false},"excerpt":{"rendered":"<p>Stargardt disease : an orphan disease \u00a0 Stargardt disease is a hereditary orphan disease which affects the macula, the central retina area. Reported for the first time by Karl Bruno Stargardt in 1909, Stargardt disease is a progressive deterioration of the macula, named macular dystrophy or maculopathy which, in most cases, appears before the age&#8230;<\/p>\n<div style=\"padding-bottom:20px; padding-top:10px;valign:middle;\" class=\"hupso-share-buttons\"><!-- Hupso Share Buttons - https:\/\/www.hupso.com\/share\/ --><a class=\"hupso_toolbar\" href=\"https:\/\/www.hupso.com\/share\/\"><img src=\"https:\/\/static.hupso.com\/share\/buttons\/share-medium.png\" style=\"border:0px; padding-top: 5px; float:left;\" alt=\"Share Button\"\/><\/a><script type=\"text\/javascript\">var hupso_services_t=new Array(\"Twitter\",\"Facebook\",\"Google Plus\",\"Linkedin\",\"Email\");var hupso_background_t=\"#EAF4FF\";var hupso_border_t=\"#66CCFF\";var hupso_toolbar_size_t=\"medium\";var hupso_image_folder_url = \"\";var hupso_url_t=\"\";var hupso_title_t=\"Understanding%20the%20disease\";<\/script><script type=\"text\/javascript\" src=\"https:\/\/static.hupso.com\/share\/js\/share_toolbar.js\"><\/script><!-- Hupso Share Buttons --><\/div>","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"open","ping_status":"open","template":"","meta":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v19.4 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Understanding the disease<\/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.stargardt.fr\/en\/understanding-the-disease\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Understanding the disease\" \/>\n<meta property=\"og:description\" content=\"Stargardt disease : an orphan disease \u00a0 Stargardt disease is a hereditary orphan disease which affects the macula, the central retina area. Reported for the first time by Karl Bruno Stargardt in 1909, Stargardt disease is a progressive deterioration of the macula, named macular dystrophy or maculopathy which, in most cases, appears before the age...\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/\" \/>\n<meta property=\"og:site_name\" content=\"Stargardt Foundation\" \/>\n<meta property=\"article:modified_time\" content=\"2015-04-08T13:52:59+00:00\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.stargardt.fr\/en\/#website\",\"url\":\"https:\/\/www.stargardt.fr\/en\/\",\"name\":\"Stargardt Foundation\",\"description\":\"Work hand in hand with research\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.stargardt.fr\/en\/?s={search_term_string}\"},\"query-input\":\"required name=search_term_string\"}],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/\",\"url\":\"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/\",\"name\":\"Understanding the disease\",\"isPartOf\":{\"@id\":\"https:\/\/www.stargardt.fr\/en\/#website\"},\"datePublished\":\"2014-03-26T21:42:23+00:00\",\"dateModified\":\"2015-04-08T13:52:59+00:00\",\"breadcrumb\":{\"@id\":\"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Accueil\",\"item\":\"https:\/\/www.stargardt.fr\/en\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Understanding the disease\"}]}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Understanding the disease","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/","og_locale":"en_US","og_type":"article","og_title":"Understanding the disease","og_description":"Stargardt disease : an orphan disease \u00a0 Stargardt disease is a hereditary orphan disease which affects the macula, the central retina area. Reported for the first time by Karl Bruno Stargardt in 1909, Stargardt disease is a progressive deterioration of the macula, named macular dystrophy or maculopathy which, in most cases, appears before the age...","og_url":"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/","og_site_name":"Stargardt Foundation","article_modified_time":"2015-04-08T13:52:59+00:00","twitter_misc":{"Est. reading time":"1 minute"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebSite","@id":"https:\/\/www.stargardt.fr\/en\/#website","url":"https:\/\/www.stargardt.fr\/en\/","name":"Stargardt Foundation","description":"Work hand in hand with research","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.stargardt.fr\/en\/?s={search_term_string}"},"query-input":"required name=search_term_string"}],"inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/","url":"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/","name":"Understanding the disease","isPartOf":{"@id":"https:\/\/www.stargardt.fr\/en\/#website"},"datePublished":"2014-03-26T21:42:23+00:00","dateModified":"2015-04-08T13:52:59+00:00","breadcrumb":{"@id":"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.stargardt.fr\/en\/understanding-the-disease\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Accueil","item":"https:\/\/www.stargardt.fr\/en\/"},{"@type":"ListItem","position":2,"name":"Understanding the disease"}]}]}},"_links":{"self":[{"href":"https:\/\/www.stargardt.fr\/en\/wp-json\/wp\/v2\/pages\/301"}],"collection":[{"href":"https:\/\/www.stargardt.fr\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.stargardt.fr\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.stargardt.fr\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.stargardt.fr\/en\/wp-json\/wp\/v2\/comments?post=301"}],"version-history":[{"count":10,"href":"https:\/\/www.stargardt.fr\/en\/wp-json\/wp\/v2\/pages\/301\/revisions"}],"predecessor-version":[{"id":1086,"href":"https:\/\/www.stargardt.fr\/en\/wp-json\/wp\/v2\/pages\/301\/revisions\/1086"}],"wp:attachment":[{"href":"https:\/\/www.stargardt.fr\/en\/wp-json\/wp\/v2\/media?parent=301"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}