{"id":1521,"date":"2024-04-25T11:05:22","date_gmt":"2024-04-25T09:05:22","guid":{"rendered":"https:\/\/www.hansegenetik.de\/general-information\/rare-diseases\/"},"modified":"2024-05-14T11:48:46","modified_gmt":"2024-05-14T09:48:46","slug":"rare-diseases","status":"publish","type":"page","link":"https:\/\/www.hansegenetik.de\/en\/general-information\/rare-diseases\/","title":{"rendered":"Rare Diseases"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"1521\" class=\"elementor elementor-1521 elementor-1434\">\n\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-60d29d3 elementor-section-full_width elementor-section-height-default elementor-section-height-default sc_fly_static\" data-id=\"60d29d3\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-extended\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-7ec0db0 sc_content_align_inherit sc_layouts_column_icons_position_left sc_fly_static\" data-id=\"7ec0db0\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-8aeab6b sc_fly_static elementor-widget elementor-widget-image\" data-id=\"8aeab6b\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"image.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<img fetchpriority=\"high\" decoding=\"async\" width=\"2042\" height=\"680\" src=\"https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases.jpg\" class=\"attachment-full size-full wp-image-1447\" alt=\"Genetische Beratung Seltene Krankheiten (Rare Diseases)\" srcset=\"https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases.jpg 2042w, https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases-360x120.jpg 360w, https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases-1920x639.jpg 1920w, https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases-768x256.jpg 768w, https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases-1536x511.jpg 1536w, https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases-370x123.jpg 370w, https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases-840x280.jpg 840w, https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases-410x137.jpg 410w\" sizes=\"(max-width: 2042px) 100vw, 2042px\" \/>\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-0031877 elementor-section-stretched scheme_default elementor-section-boxed elementor-section-height-default elementor-section-height-default sc_fly_static\" data-id=\"0031877\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;stretch_section&quot;:&quot;section-stretched&quot;,&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-wider\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-ec54732 sc_content_align_inherit sc_layouts_column_icons_position_left sc_fly_static\" data-id=\"ec54732\" data-element_type=\"column\" data-e-type=\"column\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-1956d5e sc_height_medium sc_fly_static elementor-widget elementor-widget-spacer\" data-id=\"1956d5e\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"spacer.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-spacer\">\n\t\t\t<div class=\"elementor-spacer-inner\"><\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<section class=\"elementor-section elementor-inner-section elementor-element elementor-element-4512096 elementor-section-boxed elementor-section-height-default elementor-section-height-default sc_fly_static\" data-id=\"4512096\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-no\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-inner-column elementor-element elementor-element-f306df5 sc_content_align_inherit sc_layouts_column_icons_position_left sc_fly_static\" data-id=\"f306df5\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-a086ec2 sc_fly_static elementor-widget elementor-widget-trx_sc_title\" data-id=\"a086ec2\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"trx_sc_title.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div\t\tclass=\"sc_title sc_title_default\" ><span class=\"sc_item_subtitle sc_title_subtitle sc_item_subtitle_above sc_item_title_style_default\">Hanse Genetik<\/span><h2 class=\"sc_item_title sc_title_title sc_item_title_style_default sc_item_title_tag\"\n\t\t\t><span class=\"sc_item_title_text\">Rare Diseases<\/span><\/h2><\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-c9b274b sc_fly_static elementor-widget elementor-widget-text-editor\" data-id=\"c9b274b\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<h4>Rare diseases<\/h4>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<div class=\"elementor-element elementor-element-6bc434c elementor-widget__width-initial sc_fly_static elementor-widget elementor-widget-text-editor\" data-id=\"6bc434c\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p>In the EU, a disease is considered rare if it affects no more than 500 out of 1 million people. Rare diseases often have genetic causes. Many initial symptoms can appear in childhood, while about half of rare diseases manifest in adulthood. In Germany, 4 million people suffer from a rare disease. Examples include epilepsy, Parkinson&#8217;s, dementia, or autism, as well as Crohn&#8217;s disease, Huntington&#8217;s disease, or ALS.<\/p>\n<p>On average, a person affected by a rare disease waits 4.8 years for the correct diagnosis. It is crucial to identify the causes early. Only then can affected individuals seek targeted professional treatment options and explore potential therapies. <\/p>\n<p>Our team is happy to assist you or your patients in determining whether the diagnosed condition may be genetically based. <\/p>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<section class=\"elementor-section elementor-inner-section elementor-element elementor-element-f91096d elementor-section-boxed elementor-section-height-default elementor-section-height-default sc_fly_static\" data-id=\"f91096d\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-no\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-inner-column elementor-element elementor-element-7784508 sc_content_align_inherit sc_layouts_column_icons_position_left sc_fly_static\" data-id=\"7784508\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-26f6815 sc_height_medium sc_fly_static elementor-widget elementor-widget-spacer\" data-id=\"26f6815\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"spacer.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-spacer\">\n\t\t\t<div class=\"elementor-spacer-inner\"><\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-21212b1 sc_fly_static elementor-widget elementor-widget-text-editor\" data-id=\"21212b1\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p>Hanse Genetik is a member of Nationale Allianz f\u00fcr seltene genetische Erkrankungen (NASGE)<\/p>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-29d0aeb sc_fly_static elementor-widget elementor-widget-image\" data-id=\"29d0aeb\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"image.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<a href=\"https:\/\/nasge.de\/\" target=\"_blank\">\n\t\t\t\t\t\t\t<img decoding=\"async\" width=\"319\" height=\"150\" src=\"https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/04\/Logo-NASGE.jpeg\" class=\"attachment-full size-full wp-image-1403\" alt=\"Logo-NASGE\" \/>\t\t\t\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5a0beea sc_height_medium sc_fly_static elementor-widget elementor-widget-spacer\" data-id=\"5a0beea\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"spacer.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div class=\"elementor-spacer\">\n\t\t\t<div class=\"elementor-spacer-inner\"><\/div>\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-ed7bedd sc_layouts_hide_on_wide sc_layouts_hide_on_desktop sc_layouts_hide_on_notebook sc_layouts_hide_on_tablet sc_layouts_hide_on_mobile elementor-section-boxed elementor-section-height-default elementor-section-height-default sc_fly_static\" data-id=\"ed7bedd\" data-element_type=\"section\" data-e-type=\"section\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-wider\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-42ea222 sc_content_align_inherit sc_layouts_column_icons_position_left sc_fly_static\" data-id=\"42ea222\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-7cc51f8 sc_fly_static elementor-widget elementor-widget-heading\" data-id=\"7cc51f8\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<h5 class=\"elementor-heading-title elementor-size-default\">Syndromology<\/h5>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-95fe1bc sc_fly_static elementor-widget elementor-widget-text-editor\" data-id=\"95fe1bc\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<div>\n<ul>\n<li>Aarskog Syndrome<\/li>\n<li>Angelman\/Angelman-like Syndrome<\/li>\n<li>Autism Spectrum Disorder<\/li>\n<li>Bardet-Biedl Syndrome<\/li>\n<li>Cockayne Syndrome<\/li>\n<li>Cornelia de Lange Syndrome<\/li>\n<li>Costello Syndrome<\/li>\n<li>DiGeorge Syndrome<\/li>\n<li>Ehlers-Danlos Syndrome (Vascular Form)<\/li>\n<li>Familial Hemiplegic Migraine<\/li>\n<li>Friedreich Syndrome<\/li>\n<li>Gilbert Syndrome<\/li>\n<li>Gilles de la Tourette Syndrome<\/li>\n<li>Klinefelter Syndrome<\/li>\n<li>LEOPARD Syndrome<\/li>\n<li>Cleft Lip and Palate<\/li>\n<li>Marfan Syndrome<\/li>\n<li>Microdeletion Syndromes<\/li>\n<li>Microcephaly<\/li>\n<li>Noonan Syndrome<\/li>\n<li>Rett Syndrome and Rett-like Syndrome<\/li>\n<li>Romano-Ward Syndrome<\/li>\n<li>Russell-Silver Syndrome<\/li>\n<li>Smith-Magenis Syndrome<\/li>\n<li>Walker-Warburg Syndrome<\/li>\n<li>Werner Syndrome<\/li>\n<\/ul>\n<\/div>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Hanse Genetik Rare Diseases Rare diseases In the EU, a disease is considered rare if it affects no more than 500 out of 1 million people. Rare diseases often have&hellip;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":1461,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"inline_featured_image":false,"footnotes":""},"class_list":["post-1521","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Rare Diseases - Zentrum f\u00fcr Humangenetik, Beratung, Diagnostik, Forschung - Hanse Genetik<\/title>\n<meta name=\"description\" content=\"Seltene Erkrankungen | Rare Diseases Human genetic diagnostics for genetic diseases\" \/>\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.hansegenetik.de\/en\/general-information\/rare-diseases\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Rare Diseases - Zentrum f\u00fcr Humangenetik, Beratung, Diagnostik, Forschung - Hanse Genetik\" \/>\n<meta property=\"og:description\" content=\"Seltene Erkrankungen | Rare Diseases Human genetic diagnostics for genetic diseases\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.hansegenetik.de\/en\/general-information\/rare-diseases\/\" \/>\n<meta property=\"og:site_name\" content=\"Zentrum f\u00fcr Humangenetik, Beratung, Diagnostik, Forschung - Hanse Genetik\" \/>\n<meta property=\"article:modified_time\" content=\"2024-05-14T09:48:46+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.hansegenetik.de\/wp-content\/uploads\/2024\/05\/genetische-beratung-seltene-krankheiten-rare-diseases.jpg\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/general-information\\\/rare-diseases\\\/\",\"url\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/general-information\\\/rare-diseases\\\/\",\"name\":\"Rare Diseases - Zentrum f\u00fcr Humangenetik, Beratung, Diagnostik, Forschung - Hanse Genetik\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/general-information\\\/rare-diseases\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/general-information\\\/rare-diseases\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.hansegenetik.de\\\/wp-content\\\/uploads\\\/2024\\\/05\\\/genetische-beratung-seltene-krankheiten-rare-diseases.jpg\",\"datePublished\":\"2024-04-25T09:05:22+00:00\",\"dateModified\":\"2024-05-14T09:48:46+00:00\",\"description\":\"Seltene Erkrankungen | Rare Diseases Human genetic diagnostics for genetic diseases\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/general-information\\\/rare-diseases\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/general-information\\\/rare-diseases\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/general-information\\\/rare-diseases\\\/#primaryimage\",\"url\":\"https:\\\/\\\/www.hansegenetik.de\\\/wp-content\\\/uploads\\\/2024\\\/05\\\/genetische-beratung-seltene-krankheiten-rare-diseases.jpg\",\"contentUrl\":\"https:\\\/\\\/www.hansegenetik.de\\\/wp-content\\\/uploads\\\/2024\\\/05\\\/genetische-beratung-seltene-krankheiten-rare-diseases.jpg\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/general-information\\\/rare-diseases\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"General information\",\"item\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/general-information\\\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Rare Diseases\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/#website\",\"url\":\"https:\\\/\\\/www.hansegenetik.de\\\/en\\\/\",\"name\":\"Zentrum f\u00fcr Humangenetik, Beratung, Diagnostik, Forschung - Hanse Genetik\",\"description\":\"Dr. med. 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