{"id":10872,"date":"2021-07-21T12:18:01","date_gmt":"2021-07-21T16:18:01","guid":{"rendered":"https:\/\/www.simonssearchlight.org\/?page_id=10872"},"modified":"2025-01-29T13:59:46","modified_gmt":"2025-01-29T18:59:46","slug":"csnk2b","status":"publish","type":"page","link":"https:\/\/www.simonssearchlight.org\/research\/what-we-study\/csnk2b\/","title":{"rendered":"CSNK2B"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">The information for this summary of <\/span><strong><span class=\"notranslate\">CSNK2B<\/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><strong><span class=\"notranslate\">CSNK2B<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> is also called <\/span><strong>Poirier-Bienvenu neurodevelopmental syndrome <\/strong>or <strong><span class=\"notranslate\">CSNK2B<\/span>-Related Neurodevelopmental Disorder<\/strong><span style=\"font-weight: 400;\">. For this guide, we will be using the name <\/span><strong><span class=\"notranslate\">CSNK2B<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> to encompass the wide range of variants observed in the people identified.<\/span><\/p>\n<p><a href=\"https:\/\/www.simonssearchlight.org\/gene-guide\/csnk2b\/\" target=\"_blank\" rel=\"noopener\"><b>Click here for our full CSNK2B Gene Guide<\/b><\/a><\/p>\n<p><span style=\"font-weight: 400;\">The online Gene Guide includes more information about <span class=\"notranslate\">CSNK2B<\/span> such as the chance of having another child with this condition, behavior and development concerns linked to <span class=\"notranslate\">CSNK2B<\/span>-related syndrome or specialists to consider for people with this condition. Share this resource with family members or your clinical providers.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The information for this summary of CSNK2B-related syndrome comes from research publications. This is not meant to take the place of medical advice. CSNK2B-related syndrome is also called Poirier-Bienvenu neurodevelopmental syndrome or CSNK2B-Related Neurodevelopmental Disorder. For this guide, we will be using the name CSNK2B-related syndrome to encompass the wide range of variants observed in [&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\/10872"}],"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=10872"}],"version-history":[{"count":48,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/10872\/revisions"}],"predecessor-version":[{"id":59219,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/10872\/revisions\/59219"}],"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=10872"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}