{"id":326670,"date":"2025-08-08T01:45:15","date_gmt":"2025-08-08T01:45:15","guid":{"rendered":"https:\/\/www.europesays.com\/uk\/326670\/"},"modified":"2025-08-08T01:45:15","modified_gmt":"2025-08-08T01:45:15","slug":"crispr-takes-on-the-challenge-of-rare-genetic-diseases","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/uk\/326670\/","title":{"rendered":"CRISPR takes on the challenge of rare genetic diseases"},"content":{"rendered":"<p>Rare genetic diseases are challenging for patients and their families\u2014made all the more overwhelming because symptoms tend to appear soon after birth.<\/p>\n<p>To date, there haven\u2019t been many reliable treatment options for these babies. The few that do exist involve invasive and risky procedures that don\u2019t often have a high rate of success.<\/p>\n<p>But there is a new source of hope for many of these families: the Center for Pediatric CRISPR Cures at the University of California San Francisco. The center\u2014plans for which were announced July 8\u2014is a collaboration between Jennifer Doudna, director of the Innovative Genomics Institute at the University of California, Berkeley who also earned the Nobel Prize for her work in co-discovering the gene-editing technique CRISPR, and Dr. Priscilla Chan, co-CEO and co-founder of the Chan Zuckerberg Initiative.<\/p>\n<p>Follow the latest news and policy debates on sustainable agriculture, biomedicine, and other \u2018disruptive\u2019 innovations. Subscribe to our newsletter.<\/p>\n<p>Supported by $20 million from the Chan Zuckerberg Initiative, the center focuses on treating rare genetic diseases in children, starting with a group of eight kids who will enroll in a clinical trial to access a CRISPR therapy designed specifically for them.<\/p>\n<p class=\"has-text-align-center\"><strong><a href=\"https:\/\/time.com\/7300257\/center-pediatric-crispr-cures-rare-genetic-diseases-children\/\" target=\"_blank\" rel=\"noreferrer noopener\">This is an excerpt. Read the original post here<\/a><\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"Rare genetic diseases are challenging for patients and their families\u2014made all the more overwhelming because symptoms tend to&hellip;\n","protected":false},"author":2,"featured_media":326671,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[3846],"tags":[267,70,16,15],"class_list":{"0":"post-326670","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-genetics","8":"tag-genetics","9":"tag-science","10":"tag-uk","11":"tag-united-kingdom"},"share_on_mastodon":{"url":"https:\/\/pubeurope.com\/@uk\/114990620757303808","error":""},"_links":{"self":[{"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/posts\/326670","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/comments?post=326670"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/posts\/326670\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/media\/326671"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/media?parent=326670"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/categories?post=326670"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/uk\/wp-json\/wp\/v2\/tags?post=326670"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}