{"id":8234,"date":"2020-08-28T13:11:56","date_gmt":"2020-08-28T17:11:56","guid":{"rendered":"https:\/\/www.simonssearchlight.org\/?page_id=8234"},"modified":"2025-04-08T11:20:04","modified_gmt":"2025-04-08T15:20:04","slug":"scn2a","status":"publish","type":"page","link":"https:\/\/www.simonssearchlight.org\/research\/what-we-study\/scn2a\/","title":{"rendered":"SCN2A"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">The information for this summary of <\/span><strong>SCN2A-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\/scn2a-2\/\" target=\"_blank\" rel=\"noopener\"><strong>Click here for our full SCN2A Gene Guide<\/strong><\/a><\/p>\n<p>The online Gene Guide includes more information about SCN2A such as the chance of having another child with this condition, behavior and development concerns linked to SCN2A-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\">SCN2A-related syndrome<\/span><\/strong><span style=\"font-weight: 400;\"> is also called <\/span><strong>SCN2A-developmental and epileptic encephalopathy; self-limited neonatal\/infantile epilepsy; episodic ataxia, type 9; <\/strong>and <strong>SCN2A-related disorder<\/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\">SCN2A-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 SCN2A-related syndrome comes from research publications. This is not meant to take the place of medical advice. Click here for our full SCN2A Gene Guide The online Gene Guide includes more information about SCN2A such as the chance of having another child with this condition, behavior and development concerns [&hellip;]<\/p>\n","protected":false},"author":13,"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\/8234"}],"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\/13"}],"replies":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/comments?post=8234"}],"version-history":[{"count":93,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/8234\/revisions"}],"predecessor-version":[{"id":61018,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/8234\/revisions\/61018"}],"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=8234"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}