{"id":3068,"date":"2025-10-17T14:21:25","date_gmt":"2025-10-17T18:21:25","guid":{"rendered":"https:\/\/www.med.unc.edu\/raredisease\/?page_id=3068"},"modified":"2025-11-13T12:35:08","modified_gmt":"2025-11-13T17:35:08","slug":"primary-care-the-unsung-heroes-in-rare-disease-diagnostics","status":"publish","type":"page","link":"https:\/\/www.med.unc.edu\/raredisease\/rare-disease-working-groups\/rde3\/primary-care-the-unsung-heroes-in-rare-disease-diagnostics\/","title":{"rendered":"Primary Care: The Unsung Heroes in Rare Disease Diagnostics"},"content":{"rendered":"<h1>Virtual Webinar<\/h1>\n<p class=\"paragraph\">This virtual, interactive event focuses on the diagnostic odyssey and how genetic testing can be implemented to help clinicians better support patient care. Hosted twice thus far, on October 10th and on October 30th, the presentation is geared towards primary care providers and discusses genetic basics, the benefits and limitations of genetic testing, and genetic testing available through UNC Health. Following the presentation, a panel of MDs and genetic counselors from various specialties within UNC answer questions and provide expert opinions.<\/p>\n<h3 style=\"text-align: center\">If interested, please be on the lookout for more of these events on our <a href=\"https:\/\/www.med.unc.edu\/raredisease\/news-and-events\/\">News &amp; Events page<\/a><br \/>\n(CME credit available for live event!)<\/h3>\n<h3>Recording of October 10<sup>th<\/sup> Event:<\/h3>\n<p style=\"text-align: center\">\n<!-- iframe plugin v.5.2 wordpress.org\/plugins\/iframe\/ -->\n<iframe loading=\"lazy\" src=\"https:\/\/uncch.hosted.panopto.com\/Panopto\/Pages\/Embed.aspx?id=7f694e68-7735-4917-ac4e-b379010a4098&#038;autoplay=false&#038;offerviewer=true&#038;showtitle=false&#038;showbrand=false&#038;captions=true&#038;start=0&#038;interactivity=all\" height=\"400\" width=\"850\" style=\"border: 1px solid #464646;\" 0=\"allowfullscreen\" allow=\"autoplay\" title=\"Primary Care: The Unsung Heroes in Rare Disease Diagnostics\" scrolling=\"yes\" class=\"iframe-class\" frameborder=\"0\"><\/iframe>\n\n<h3>Recording of October 30<sup>th<\/sup> Event:<\/h3>\n<p style=\"text-align: center\">\n<!-- iframe plugin v.5.2 wordpress.org\/plugins\/iframe\/ -->\n<iframe loading=\"lazy\" src=\"https:\/\/uncch.hosted.panopto.com\/Panopto\/Pages\/Embed.aspx?id=7102801d-25bc-4493-81da-b38a01135755&#038;autoplay=false&#038;offerviewer=true&#038;showtitle=false&#038;showbrand=false&#038;captions=true&#038;start=0&#038;interactivity=all\" height=\"400\" width=\"850\" style=\"border: 1px solid #464646;\" 0=\"allowfullscreen\" allow=\"autoplay\" title=\"Primary Care: The Unsung Heroes in Rare Disease Diagnostics\" scrolling=\"yes\" class=\"iframe-class\" frameborder=\"0\"><\/iframe>\n\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Virtual Webinar This virtual, interactive event focuses on the diagnostic odyssey and how genetic testing can be implemented to help clinicians better support patient care. Hosted twice thus far, on October 10th and on October 30th, the presentation is geared towards primary care providers and discusses genetic basics, the benefits and limitations of genetic testing, &hellip; <a href=\"https:\/\/www.med.unc.edu\/raredisease\/rare-disease-working-groups\/rde3\/primary-care-the-unsung-heroes-in-rare-disease-diagnostics\/\" aria-label=\"Read more about Primary Care: The Unsung Heroes in Rare Disease Diagnostics\">Read more<\/a><\/p>\n","protected":false},"author":85590,"featured_media":0,"parent":2389,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"layout":"","cellInformation":"","apiCallInformation":"","footnotes":"","_links_to":"","_links_to_target":""},"class_list":["post-3068","page","type-page","status-publish","hentry","odd"],"acf":[],"_links_to":[],"_links_to_target":[],"_links":{"self":[{"href":"https:\/\/www.med.unc.edu\/raredisease\/wp-json\/wp\/v2\/pages\/3068","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.med.unc.edu\/raredisease\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.med.unc.edu\/raredisease\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/raredisease\/wp-json\/wp\/v2\/users\/85590"}],"replies":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/raredisease\/wp-json\/wp\/v2\/comments?post=3068"}],"version-history":[{"count":8,"href":"https:\/\/www.med.unc.edu\/raredisease\/wp-json\/wp\/v2\/pages\/3068\/revisions"}],"predecessor-version":[{"id":3098,"href":"https:\/\/www.med.unc.edu\/raredisease\/wp-json\/wp\/v2\/pages\/3068\/revisions\/3098"}],"up":[{"embeddable":true,"href":"https:\/\/www.med.unc.edu\/raredisease\/wp-json\/wp\/v2\/pages\/2389"}],"wp:attachment":[{"href":"https:\/\/www.med.unc.edu\/raredisease\/wp-json\/wp\/v2\/media?parent=3068"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}