{"id":1096,"date":"2025-11-07T09:26:12","date_gmt":"2025-11-07T08:26:12","guid":{"rendered":"https:\/\/genomapp.com\/?p=1096"},"modified":"2026-02-06T17:50:47","modified_gmt":"2026-02-06T16:50:47","slug":"featured-condition-ehlers-danlos-syndrome","status":"publish","type":"post","link":"https:\/\/genomapp.com\/en\/featured-condition-ehlers-danlos-syndrome\/","title":{"rendered":"Featured Condition: Ehlers-Danlos Syndrome"},"content":{"rendered":"\n<p class=\"has-medium-font-size\">To mark the Genomapp&#8217;s <a href=\"https:\/\/genomapp.com\/en\/a-decade-decoding-the-future-of-your-health\/\">10th anniversary<\/a> we&#8217;re introducing the new Featured Condition section. The first condition featured is Ehlers-Danlos syndrome.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"683\" src=\"https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/pattern_zebra-opt-1024x683.webp\" alt=\"\" class=\"wp-image-1103\" srcset=\"https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/pattern_zebra-opt-1024x683.webp 1024w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/pattern_zebra-opt-300x200.webp 300w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/pattern_zebra-opt-768x512.webp 768w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/pattern_zebra-opt-1536x1024.webp 1536w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/pattern_zebra-opt-2048x1365.webp 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n\n\n<p>Ehlers-Danlos syndrome (EDS) is not a single disease but a group of 13 distinct hereditary disorders that share characteristics such as joint hyperlaxity, skin hyperextensibility, and tissue fragility. These syndromes are due to genetic changes that affect connective tissue, which provides support and structure to the entire body.<\/p>\n\n\n\n<p>Ehlers-Danlos syndrome is caused by inherited mutations in genes that encode collagen or related proteins. These mutations affect the strength and elasticity of connective tissues. Mutations in various genes such as COL5A1, COL5A2, and COL3A1 have been identified, depending on the specific type of EDS.&nbsp;<\/p>\n\n\n\n<p>Most common EDS symptoms:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Joint Hypermobility<\/li>\n\n\n\n<li>Skin Hyperextensibility<\/li>\n\n\n\n<li>Fragile Skin<\/li>\n\n\n\n<li>Chronic Pain<\/li>\n\n\n\n<li>Fatigue<\/li>\n\n\n\n<li>Digestive Problems<\/li>\n\n\n\n<li>Dizziness and Tachycardia on Standing<\/li>\n\n\n\n<li>Abnormal Scarring<\/li>\n\n\n\n<li>Frequent Joint Dislocations<\/li>\n\n\n\n<li>Cardiovascular Problems<\/li>\n<\/ul>\n\n\n\n<p>Since EDS is genetic, it can\u2019t be prevented, but you can take steps to avoid complications and feel better day-to-day.<\/p>\n\n\n\n<p>Living with EDS can be challenging, and support from others who understand the condition is invaluable. Among the resources and organizations related to EDS we can mention <a href=\"https:\/\/www.ehlers-danlos.com\/\">The Ehlers-Danlos Society<\/a>: Global organization dedicated to research, education, and support for individuals with EDS and hypermobility spectrum disorders. <\/p>\n\n\n\n<p>More information in <a href=\"https:\/\/genomapp.com\/en\/download\/\">Genomapp&#8217;s app<\/a>. Discover what your DNA says about your predisposition to this condition.<\/p>\n\n\n\n<figure class=\"wp-block-gallery has-nested-images columns-default is-cropped wp-block-gallery-1 is-layout-flex wp-block-gallery-is-layout-flex\">\n<figure class=\"wp-block-image size-large has-custom-border\"><img loading=\"lazy\" decoding=\"async\" width=\"493\" height=\"1024\" data-id=\"1109\" src=\"https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-493x1024.webp\" alt=\"\" class=\"wp-image-1109\" style=\"border-width:1px\" srcset=\"https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-493x1024.webp 493w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-144x300.webp 144w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-768x1596.webp 768w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-739x1536.webp 739w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-985x2048.webp 985w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos.webp 1157w\" sizes=\"auto, (max-width: 493px) 100vw, 493px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large has-custom-border\"><img loading=\"lazy\" decoding=\"async\" width=\"494\" height=\"1024\" data-id=\"1106\" src=\"https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-reveal-494x1024.webp\" alt=\"\" class=\"wp-image-1106\" style=\"border-width:1px\" srcset=\"https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-reveal-494x1024.webp 494w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-reveal-145x300.webp 145w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-reveal-768x1593.webp 768w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-reveal-741x1536.webp 741w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-reveal-987x2048.webp 987w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-reveal.webp 1163w\" sizes=\"auto, (max-width: 494px) 100vw, 494px\" \/><\/figure>\n\n\n\n<figure class=\"wp-block-image size-large has-custom-border\"><img loading=\"lazy\" decoding=\"async\" width=\"491\" height=\"1024\" data-id=\"1105\" src=\"https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-results-491x1024.webp\" alt=\"\" class=\"wp-image-1105\" style=\"border-width:1px\" srcset=\"https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-results-491x1024.webp 491w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-results-144x300.webp 144w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-results-768x1600.webp 768w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-results-737x1536.webp 737w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-results-983x2048.webp 983w, https:\/\/genomapp.com\/wp-content\/uploads\/2025\/11\/genomapp-ehlers-danlos-results.webp 1156w\" sizes=\"auto, (max-width: 491px) 100vw, 491px\" \/><\/figure>\n<\/figure>\n","protected":false},"excerpt":{"rendered":"<p>To mark the Genomapp&#8217;s 10th anniversary we&#8217;re introducing the new Featured Condition section. The first condition featured is Ehlers-Danlos syndrome. Ehlers-Danlos syndrome (EDS) is not a single disease but a group of 13 distinct hereditary disorders that share characteristics such as joint hyperlaxity, skin hyperextensibility, and tissue fragility. These syndromes are due to genetic changes [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[7],"tags":[],"class_list":["post-1096","post","type-post","status-publish","format-standard","hentry","category-featured-condition"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Featured Condition: Ehlers-Danlos Syndrome - genomapp.com<\/title>\n<meta name=\"description\" content=\"Ehlers-Danlos syndrome is not a single disease but a group of 13 distinct hereditary disorders. EDS syndrome is caused by inherited mutations.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/genomapp.com\/en\/featured-condition-ehlers-danlos-syndrome\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Featured Condition: Ehlers-Danlos Syndrome - genomapp.com\" \/>\n<meta property=\"og:description\" content=\"Ehlers-Danlos syndrome is not a single disease but a group of 13 distinct hereditary disorders. 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