{"id":9452,"date":"2020-11-23T15:39:42","date_gmt":"2020-11-23T20:39:42","guid":{"rendered":"https:\/\/www.simonssearchlight.org\/?page_id=9452"},"modified":"2025-01-29T14:08:53","modified_gmt":"2025-01-29T19:08:53","slug":"dync1h1","status":"publish","type":"page","link":"https:\/\/www.simonssearchlight.org\/research\/what-we-study\/dync1h1\/","title":{"rendered":"DYNC1H1"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">The information for this summary of <\/span><strong><span class=\"notranslate\">DYNC1H1<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> comes from research publications. This is not meant to take the place of medical advice.<\/span><\/p>\n<p><a href=\"https:\/\/www.simonssearchlight.org\/gene-guide\/dync1h1\/\" target=\"_blank\" rel=\"noopener\"><strong>Click here for our full DYNC1H1 Gene Guide<\/strong><\/a><\/p>\n<p>The online Gene Guide includes more information about <span class=\"notranslate\">DYNC1H1<\/span> such as the chance of having another child with this condition, behavior and development concerns linked to <span class=\"notranslate\">DYNC1H1<\/span>-related syndrome or specialists to consider for people with this condition. Share this resource with family members or your clinical providers.<\/p>\n<p><strong><span class=\"notranslate\">DYNC1H1<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> is also called <\/span><strong>Charcot-Marie-Tooth disease<\/strong>, <strong>Complex cortical dysplasia with other brain malformations<\/strong><span style=\"font-weight: 400;\">, or <\/span><strong>Spinal muscular atrophy with lower extremity predominance<\/strong><span style=\"font-weight: 400;\">. For this guide, we will be using the name <\/span><strong><span class=\"notranslate\">DYNC1H1<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> to encompass the wide range of variants observed in the people identified.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The information for this summary of DYNC1H1-related syndrome comes from research publications. This is not meant to take the place of medical advice. Click here for our full DYNC1H1 Gene Guide The online Gene Guide includes more information about DYNC1H1 such as the chance of having another child with this condition, behavior and development concerns [&hellip;]<\/p>\n","protected":false},"author":6,"featured_media":0,"parent":29,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-gene-card.php","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","footnotes":""},"acf":[],"_links":{"self":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/9452"}],"collection":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/users\/6"}],"replies":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/comments?post=9452"}],"version-history":[{"count":31,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/9452\/revisions"}],"predecessor-version":[{"id":59233,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/9452\/revisions\/59233"}],"up":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/29"}],"wp:attachment":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/media?parent=9452"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}