{"id":8173,"date":"2020-08-07T16:47:36","date_gmt":"2020-08-07T20:47:36","guid":{"rendered":"https:\/\/www.simonssearchlight.org\/?page_id=8173"},"modified":"2025-01-29T14:48:16","modified_gmt":"2025-01-29T19:48:16","slug":"syngap1","status":"publish","type":"page","link":"https:\/\/www.simonssearchlight.org\/research\/what-we-study\/syngap1\/","title":{"rendered":"SYNGAP1"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">The information for this summary of <\/span><strong>SYNGAP1-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\/syngap1\/\" target=\"_blank\" rel=\"noopener\"><strong>Click here to view the full SYNGAP1 Gene Guide<\/strong> <\/a><\/p>\n<p>The online Gene Guide includes more information about SYNGAP1 such as the chance of having another child with this condition, behavior and development concerns linked to SYNGAP1-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\">SYNGAP1-related syndrome<\/span><\/strong><span style=\"font-weight: 400;\"> is also called<\/span> <strong>SYNGAP1-related intellectual disability (SYNGAP1-ID) <\/strong>or <strong>intellectual developmental disorder, autosomal dominant 5<\/strong><span style=\"font-weight: 400;\">.<\/span> <span style=\"font-weight: 400;\">For this webpage, we will be using the name <\/span><strong><span class=\"notranslate\">SYNGAP1-related syndrome<\/span><\/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 SYNGAP1-related syndrome comes from research publications. This is not meant to take the place of medical advice. Click here to view the full SYNGAP1 Gene Guide The online Gene Guide includes more information about SYNGAP1 such as the chance of having another child with this condition, behavior and development [&hellip;]<\/p>\n","protected":false},"author":18,"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\/8173"}],"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\/18"}],"replies":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/comments?post=8173"}],"version-history":[{"count":55,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/8173\/revisions"}],"predecessor-version":[{"id":59289,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/8173\/revisions\/59289"}],"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=8173"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}